Acetyl-coa carboxylase modulators

ABSTRACT

Provided herein are compounds that exhibit activity as acetyl-CoA carboxylase modulators (e.g., inhibitors) and are useful, for example, in methods for the control of fungal pathogens in plants.

FIELD

Provided herein are compounds that exhibit activity as acetyl-CoAcarboxylase modulators (e.g., inhibitors) and are useful, for example,in methods for the control of fungal pathogens and diseases caused byfungal pathogens in plants.

BACKGROUND

Acetyl-CoA carboxylase (“ACCase”) is an essential catalyst for therate-limiting step of fatty acid biosynthesis in both eukaryotes andprokaryotes. Phytopathogenic fungi can infect crop plants either in thefield or after harvesting, resulting in considerable economic losses tofarmers and producers worldwide. In addition to the agricultural impact,when food and feed contaminated with fungi or the toxins they produceare ingested by humans or livestock, a number of debilitating diseasesor death can occur. Approximately 10,000 species of fungi are known todamage crops and affect quality and yield. Crop rotation, breeding ofresistant cultivars, the application of agrochemicals and combinationsof these strategies is commonly employed to stem the spread of fungalpathogens and the diseases they cause. Additional chemistry and methodsof using such as a modulator for ACCase or to control fungi areimportant for, among other things, protection in agriculture.

For example, the rapid onset of resistance to chemical fungicides hasoften lowered the efficacy of some chemical fungicides. This threat, aswell as emergence and spread of additional fungal diseases, accentuatesthe need for new means of fungal control.

SUMMARY

In one aspect, therefore, the present disclosure is directed to acompound of Formula I or a salt thereof,

wherein

R¹ is selected from the group consisting of OH, and N(R⁷R⁸), wherein R⁷and R⁸ are independently selected from the group consisting of hydrogen,OH, and CH₃;

R² is selected from the group consisting of alkyl, cycloalkyl,heterocycloalkyl, aryl, and heteroaryl, each of which may be optionallysubstituted with one or more substituents selected from the groupconsisting of halogen, CH₃, OCH₃, CF₃, OCF₃, and CN;

R³ is selected from the group consisting of hydrogen, CN, ethynyl,CH₂N(R⁹R¹⁰), and) C(O)N(R⁹R¹⁰), wherein R⁹ and R¹⁰ are eachindependently selected from the group consisting of hydrogen and alkyl;

R⁴ is selected from the group consisting of haloalkyl, aryl, arylalkyl,heteroaryl, and heteroarylalkyl, each of which may be optionallyindependently substituted with one or more substitutents selected fromthe group consisting of halogen, alkyl, alkoxy, haloalkyl, haloalkoxy,alkenyl, hydroxyalky, hydroxy, N(R⁹R¹⁰), NR¹¹C(O)R¹², and O(CO)R¹³,wherein R⁹ and R¹⁰ are independently selected from the group consistingof hydrogen and alkyl, R¹¹ is selected from the group consisting ofhydrogen and alkyl, R¹² is alkyl, and R¹³ is alkyl;

R⁵ is selected from the group consisting of hydrogen and alkyl; or R⁴and R⁵ together form a fused cycloalkyl or heterocycloalkyl ring havingfrom 5 to 6 ring atoms selected from the group consisting of carbon,nitrogen, and oxygen;

R⁶ is selected from the group consisting of alkyl, haloalkyl, aryl,arylalkyl, heteroaryl, and heteroarylalkyl, each of which may beoptionally independently substituted with one or more substitutentsselected from the group consisting of halogen, alkyl, alkoxy, haloalkyl,and haloalkoxy; or

R⁵ and R⁶ together form a fused cycloalkyl or heterocycloalkyl ringhaving from 5 to 6 ring atoms selected from the group consisting ofcarbon, nitrogen, and oxygen; and

E is selected from the group consisting of S, O, N(H), N(CH₃), and CH₂.

In another aspect, the present disclosure is directed to a compound ofFormula II or a salt thereof,

wherein

R¹ is selected from the group consisting of a prodrug of a carboxylicacid and a carboxylic acid isostere;

R² is selected from the group consisting of alkyl, cycloalkyl,heterocycloalkyl, aryl and heteroaryl, each of which may be optionallyindependently substituted with one or more substituents selected fromthe group consisting of halogen, CH₃, OCH₃, CF₃, OCF₃, and CN;

R³ is selected from the group consisting of hydrogen, CN, ethynyl,CH₂N(R⁹R¹⁰), and C(O)N(R⁹R¹⁰), wherein R⁹ and R¹⁰ are each independentlyselected from the group consisting of hydrogen and alkyl;

R⁴ is selected from the group consisting of haloalkyl, aryl, arylalkyl,heteroaryl, and heteroarylalkyl, each of which may be optionallyindependently substituted with one or more substitutents selected fromthe group consisting of halogen, alkyl, alkoxy, haloalkyl, haloalkoxy,alkenyl, hydroxyalkyl, hydroxyl, N(R⁹R¹⁰), NR¹¹C(O)R¹² and O(CO)R¹³,wherein R⁹ and R¹⁰ are independently selected from the group consistingof hydrogen and alkyl, R¹¹ is selected from the group consisting ofhydrogen and alkyl, R¹² is alkyl, and R¹³ is alkyl;

R⁵ is selected from the group consisting of hydrogen and alkyl; or R⁴and R⁵ together form a fused cycloalkyl or heterocycloalkyl ring havingfrom 5 to 6 ring atoms selected from the group consisting of carbon,nitrogen, and oxygen;

R⁶ is selected from the group consisting of alkyl, haloalkyl, aryl,arylalkyl, heteroaryl, and heteroarylalkyl, each of which may beoptionally independently substituted with one or more substitutentsselected from the group consisting of halogen, alkyl, alkoxy, haloalkyl,and haloalkoxy; or R⁵ and R⁶ together form a fused cycloalkyl orheterocycloalkyl ring having from 5 to 6 ring atoms selected from thegroup consisting of carbon, nitrogen, and oxygen; and

E is selected from the group consisting of S, O, N(H), N(CH₃), and CH₂.

Another aspect of the present disclosure is directed to a compoundselected from the group consisting of:2-((4-(4-chlorophenyl)-3-cyano-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-(thiophen-2-yl)-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4,6-di(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetic acid,or a salt thereof,2-((3-cyano-4-phenyl-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-6-phenylpyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-methyl-4-(thiophen-2-yl)-5,6,7,8-tetrahydro-1,6-naphthyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((4-cyano-1-(thiophen-2-yl)-5,6,7,8-tetrahydroisoquinolin-3-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-(2,4-dimethoxyphenyl)-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-(3,4-dimethoxyphenyl)-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((6-(4-bromophenyl)-3-cyano-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-(furan-2-yl)-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4,6-diphenylpyridin-2-yl)thio)-2-phenylacetic acid, or asalt thereof,2-((3-cyano-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((4-cyano-1-ethyl-5,6,7,8-tetrahydroisoquinolin-3-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-methyl-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-phenyl-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylaceticacid or a salt thereof,2-((4-(4-chlorophenyl)-3-cyano-5,6,7,8-tetrahydronaphthalen-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-(furan-2-yl)-4-(4-methoxyphenyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-(thiophen-2-yl)-4-(p-tolyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-(4-fluorophenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((4-(4-bromophenyl)-3-cyano-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-(furan-2-yl)-4-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4,6-di(furan-2-yl)pyridin-2-yl)thio)-2-phenylacetic acid, ora salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinolin-2-yl)oxy)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-6-(1-oxidothiophen-2-yl)pyridin-2-yl)oxy)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)butanoicacid, or a salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-6-(pyrimidin-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-(3-methoxy-1-methyl-1H-pyrrol-2-yl)-4-(4-methoxyphenyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-(furan-2-yl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylacetamide,or a salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetamide,or a salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-N-hydroxy-2-phenylacetamide,or a salt thereof,4-(4-methoxyphenyl)-2-((phenyl(1H-tetrazol-5-yl)methyl)thio)-6-(thiophen-2-yl)nicotinonitrile,or a salt thereof,(((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)(phenyl)methyl)phosphonicacid, or a salt thereof,(((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)(phenyl)methyl)phosphinicacid, or a salt thereof,((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)(phenyl)methanesulfonicacid, or a salt thereof,((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)(phenyl)methanesulfonamide,or a salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-N-(methylsulfonyl)-2-phenylacetamide,or a salt thereof,2-(((2,4-dioxothiazolidin-5-yl)(phenyl)methyl)thio)-4-(4-methoxyphenyl)-6-(thiophen-2-yl)nicotinonitrile,or a salt thereof,2-(((2,4-dioxooxazolidin-5-yl)(phenyl)methyl)thio)-4-(4-methoxyphenyl)-6-(thiophen-2-yl)nicotinonitrile,or a salt thereof,4-(4-methoxyphenyl)-2-(((5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)(phenyl)methyl)thio)-6-(thiophen-2-yl)nicotinonitrile,or a salt thereof,2-((2-hydroxy-1-phenylethyl)thio)-4-(4-methoxyphenyl)-6-(thiophen-2-yl)nicotinonitrile,or a salt thereof,2-((2-hydroxy-1-phenylethyl)thio)-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinoline-3-carbonitrile,or a salt thereof, methyl2-((3-cyano-6-(thiophen-2-yl)-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylacetate,or a salt thereof, and4-(furan-2-yl)-2-((2-hydroxy-1-phenylethyl)thio)-6-(thiophen-2-yl)nicotinonitrile,or a salt thereof.

Another aspect of the present disclosure is generally related to amethod of controlling fungal pathogens comprising administering to aplant, a seed or soil a composition comprising an effective amount of acompound as described herein.

Another aspect of the present disclosure is generally related to amethod for modulating ACCase in a biological organism comprisingadministering to the biological organism a composition comprising aneffective amount of a compound as described herein.

Another aspect of the present disclosure is generally related to acomposition comprising a compound as described herein.

Another aspect of the present disclosure is generally related to a seedcomprising a coating comprising a compound or a composition as describedherein.

Other objects and features will be in part apparent and in part pointedout hereinafter.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 depicts the ORTEP plots (50% probability ellipsoids) for acompound of Formula Ia-ii-e2 using single crystal X-ray diffraction.

DETAILED DESCRIPTION

Described herein are compounds that exhibit activity as acetyl-CoAcarboxylase modulators. The compounds described herein may be used, forexample, in the preparation of compositions and in accordance withmethods for control of fungal pathogens, as set forth in detail below.

For example, in one embodiment, the compound is a compound of Formula Ior a salt thereof,

wherein

R¹ is selected from the group consisting of OH and N(R⁷R⁸), wherein R⁷and R⁸ are independently selected from the group consisting of hydrogen,OH, and CH₃;

R² is selected from the group consisting of alkyl, cycloalkyl,heterocycloalkyl, aryl, and heteroaryl, each of which may be optionallysubstituted with one or more substituents selected from the groupconsisting of halogen, CH₃, OCH₃, CF₃, OCF₃, and CN;

R³ is selected from the group consisting of hydrogen, CN, ethynyl,CH₂N(R⁹R¹⁰), and C(O)N(R⁹R¹⁰), wherein R⁹ and R¹⁰ are each independentlyselected from the group consisting of hydrogen and alkyl;

R⁴ is selected from the group consisting of haloalkyl, aryl, arylalkyl,heteroaryl, and heteroarylalkyl, each of which may be optionallyindependently substituted with one or more substitutents selected fromthe group consisting of halogen, alkyl, alkoxy, haloalkyl, haloalkoxy,alkenyl, hydroxyalky, hydroxy, N(R⁹R¹⁰), NR¹¹C(O)R¹², and O(CO)R¹³,wherein R⁹ and R¹⁰ are independently selected from the group consistingof hydrogen and alkyl, R¹¹ is selected from the group consisting ofhydrogen and alkyl, R¹² is alkyl, and R¹³ is alkyl;

R⁵ is selected from the group consisting of hydrogen and alkyl; or R⁴and R⁵ together form a fused cycloalkyl or heterocycloalkyl ring havingfrom 5 to 6 ring atoms selected from the group consisting of carbon,nitrogen, and oxygen;

R⁶ is selected from the group consisting of alkyl, haloalkyl, aryl,arylalkyl, heteroaryl, and heteroarylalkyl, each of which may beoptionally independently substituted with one or more substitutentsselected from the group consisting of halogen, alkyl, alkoxy, haloalkyl,and haloalkoxy; or

R⁵ and R⁶ together form a fused cycloalkyl or heterocycloalkyl ringhaving from 5 to 6 ring atoms selected from the group consisting ofcarbon, nitrogen, and oxygen; and

E is selected from the group consisting of S, O, N(H), N(CH₃), and CH₂.

In some embodiments, the compound is a compound of Formula I wherein R¹is OH and R² is selected from the group consisting of aryl andheteroaryl.

For example, the compound of Formula I may be a compound of Formula Iaor a salt thereof,

wherein

R² is selected from the group consisting of alkyl, cycloalkyl,heterocycloalkyl, aryl and heteroaryl, each of which may be optionallyindependently substituted with one or more substituents selected fromthe group consisting of halogen, CH₃, OCH₃, CF₃, OCF₃, and CN;

R³ is selected from the group consisting of hydrogen, CN, ethynyl,CH₂N(R⁹R¹⁰), and C(O)N(R⁹R¹⁰), wherein R⁹ and R¹⁰ are each independentlyselected from the group consisting of hydrogen and alkyl;

R⁴ is selected from the group consisting of haloalkyl, aryl, arylalkyl,heteroaryl, and heteroarylalkyl, each of which may be optionallyindependently substituted with one or more substitutents selected fromthe group consisting of halogen, alkyl, alkoxy, haloalkyl, haloalkoxy,alkenyl, hydroxyalky, hydroxy, N(R⁹R¹⁰), NR¹¹C(O)R¹² and O(CO)R¹³,wherein R⁹ and R¹⁰ are independently selected from the group consistingof hydrogen and alkyl, R¹¹ is selected from the group consisting ofhydrogen and alkyl, R¹² is alkyl, and R¹³ is alkyl;

R⁵ is selected from the group consisting of hydrogen and alkyl; or R⁴and R⁵ together form a fused cycloalkyl or heterocycloalkyl ring havingfrom 5 to 6 ring atoms selected from the group consisting of carbon,nitrogen, and oxygen;

R⁶ is selected from the group consisting of alkyl, haloalkyl, aryl,arylalkyl, heteroaryl, and heteroarylalkyl, each of which may beoptionally independently substituted with one or more substitutentsselected from the group consisting of halogen, alkyl, alkoxy, haloalkyl,and haloalkoxy; or R⁵ and R⁶ together form a fused cycloalkyl orheterocycloalkyl ring having from 5 to 6 ring atoms selected from thegroup consisting of carbon, nitrogen, and oxygen; and

E is selected from the group consisting of S, O, N(H), N(CH₃), and CH₂.

In some embodiments, the compound of Formula I may be a compound ofFormula Ib or a salt thereof,

wherein

R² is selected from the group consisting of alkyl, cycloalkyl,heterocycloalkyl, aryl and heteroaryl, each of which may be optionallyindependently substituted with one or more substituents selected fromthe group consisting of halogen, CH₃, OCH₃, CF₃, OCF₃, and CN;

R³ is selected from the group consisting of hydrogen, CN, ethynyl,CH₂N(R⁹R¹⁰), and C(O)N(R⁹R¹⁰), wherein R⁹ and R¹⁰ are each independentlyselected from the group consisting of hydrogen and alkyl;

R⁴ is selected from the group consisting of haloalkyl, aryl, arylalkyl,heteroaryl, and heteroarylalkyl, each of which may be optionallyindependently substituted with one or more substitutents selected fromthe group consisting of halogen, alkyl, alkoxy, haloalkyl, haloalkoxy,alkenyl, hydroxyalkyl, hydroxyl, N(R⁹R¹⁰), NR¹¹C(O)R¹², and O(CO)R¹³,wherein R⁹ and R¹⁰ are independently selected from the group consistingof hydrogen and alkyl, R¹¹ is selected from the group consisting ofhydrogen and alkyl, R¹² is alkyl, and R¹³ is alkyl;

R⁵ is selected from the group consisting of hydrogen and alkyl; or R⁴and R⁵ together form a fused cycloalkyl or heterocycloalkyl ring havingfrom 5 to 6 ring atoms selected from the group consisting of carbon,nitrogen, and oxygen;

R⁶ is selected from the group consisting of alkyl, haloalkyl, aryl,arylalkyl, heteroaryl, and heteroarylalkyl, each of which may beoptionally independently substituted with one or more substitutentsselected from the group consisting of halogen, alkyl, alkoxy, haloalkyl,and haloalkoxy; or R⁵ and R⁶ together form a fused cycloalkyl orheterocycloalkyl ring having from 5 to 6 ring atoms selected from thegroup consisting of carbon, nitrogen, and oxygen;

R⁷ and R⁸ are independently selected from the group consisting ofhydrogen, OH, and CH₃; and

E is selected from the group consisting of S, O, N(H), N(CH₃), and CH₂.

In some embodiments, the compound is a compound of Formula I wherein R¹is OH.

In some embodiments, the compound is a compound of Formula I, Ia, or Ibwherein R² is phenyl. In another embodiment, the compound is a compoundof Formula I, Ia, or Ib wherein R² is alkyl. In other embodiments, thecompound may be a compound of Formula I, Ia, or Ib wherein R² isunsubstituted heteroaryl. For example, R² may be pyridyl, pyrimidyl(e.g., 2,6-pyrimidyl), or thienyl (e.g., 2-thienyl).

In some embodiments, the compound is a compound of Formula I, Ia, or Ibwherein R³ is CN.

In some embodiments, the compound is a compound of Formula I, Ia, or Ibwherein R⁴ is selected from the group consisting of CF₃, thienyl, andoptionally substituted phenyl. For example, R⁴ may be 4-halophenyl(e.g., 4-chlorophenyl) or 4-alkoxyphenyl (e.g., 4-methoxyphenyl).

In some embodiments, the compound is a compound of Formula I, Ia, or Ibwherein R⁵ is hydrogen.

In some embodiments, the compound is a compound of Formula I, Ia, or Ibwherein R⁶ is selected from the group consisting of methyl, ethyl,thienyl, furanyl, and optionally substituted phenyl. In one embodiment,R⁶ may be 4-halophenyl (e.g., 4-bromophenyl) or 4-alkoxyphenyl (e.g.,4-methoxyphenyl). In some embodiments, R⁶ may be disubstituted phenyl(e.g., 2,4-disubstituted phenyl or 3,4-disubstituted phenyl). In oneembodiment, R⁶ may be 2,4-dimethoxyphenyl or 3,4-dimethoxyphenyl.

In some embodiments, the compound is a compound of Formula I, Ia, or Ibwherein E is selected from the group consisting of S, O, and CH₂. Forexample, E may be S.

In another embodiment, the compound is a compound of Formula II or asalt thereof,

wherein

R¹ is selected from the group consisting of a prodrug of a carboxylicacid and a carboxylic acid isostere;

R² is selected from the group consisting of alkyl, cycloalkyl,heterocycloalkyl, aryl and heteroaryl, each of which may be optionallyindependently substituted with one or more substituents selected fromthe group consisting of halogen, CH₃, OCH₃, CF₃, OCF₃, and CN;

R³ is selected from the group consisting of hydrogen, CN, ethynyl,CH₂N(R⁹R¹⁰), and C(O)N(R⁹R¹⁰), wherein R⁹ and R¹⁰ are each independentlyselected from the group consisting of hydrogen and alkyl;

R⁴ is selected from the group consisting of haloalkyl, aryl, arylalkyl,heteroaryl, and heteroarylalkyl, each of which may be optionallyindependently substituted with one or more substitutents selected fromthe group consisting of halogen, alkyl, alkoxy, haloalkyl, haloalkoxy,alkenyl, hydroxyalky, hydroxy, N(R⁹R¹⁰), NR¹¹C(O)R¹² and O(CO)R¹³,wherein R⁹ and R¹⁰ are independently selected from the group consistingof hydrogen and alkyl, R¹¹ is selected from the group consisting ofhydrogen and alkyl, R¹² is alkyl, and R¹³ is alkyl;

R⁵ is selected from the group consisting of hydrogen and alkyl; or R⁴and R⁵ together form a fused cycloalkyl or heterocycloalkyl ring havingfrom 5 to 6 ring atoms selected from the group consisting of carbon,nitrogen, and oxygen;

R⁶ is selected from the group consisting of alkyl, haloalkyl, aryl,arylalkyl, heteroaryl, and heteroarylalkyl, each of which may beoptionally independently substituted with one or more substitutentsselected from the group consisting of halogen, alkyl, alkoxy, haloalkyl,and haloalkoxy; or R⁵ and R⁶ together form a fused cycloalkyl orheterocycloalkyl ring having from 5 to 6 ring atoms selected from thegroup consisting of carbon, nitrogen, and oxygen; and

E is selected from the group consisting of S, O, N(H), N(CH₃), and CH₂.

For example, the compound of Formula II may be a compound of Formula IIaor a salt thereof,

wherein

R¹ is a carboxylic acid isostere;

R² is selected from the group consisting of alkyl, cycloalkyl,heterocycloalkyl, aryl and heteroaryl, each of which may be optionallyindependently substituted with one or more substituents selected fromthe group consisting of halogen, CH₃, OCH₃, CF₃, OCF₃, and CN;

R³ is selected from the group consisting of hydrogen, CN, ethynyl,CH₂N(R⁹R¹⁰), and C(O)N(R⁹R¹⁰), wherein R⁹ and R¹⁰ are each independentlyselected from the group consisting of hydrogen and alkyl;

R⁴ is selected from the group consisting of haloalkyl, aryl, arylalkyl,heteroaryl, and heteroarylalkyl, each of which may be optionallyindependently substituted with one or more substitutents selected fromthe group consisting of halogen, alkyl, alkoxy, haloalkyl, haloalkoxy,alkenyl, hydroxyalky, hydroxy, N(R⁹R¹⁰), NR¹¹C(O)R¹² and O(CO)R¹³,wherein R⁹ and R¹⁰ are independently selected from the group consistingof hydrogen and alkyl, R¹¹ is selected from the group consisting ofhydrogen and alkyl, R¹² is alkyl, and R¹³ is alkyl;

R⁵ is selected from the group consisting of hydrogen and alkyl; or R⁴and R⁵ together form a fused cycloalkyl or heterocycloalkyl ring havingfrom 5 to 6 ring atoms selected from the group consisting of carbon,nitrogen, and oxygen;

R⁶ is selected from the group consisting of alkyl, haloalkyl, aryl,arylalkyl, heteroaryl, and heteroarylalkyl, each of which may beoptionally independently substituted with one or more substitutentsselected from the group consisting of halogen, alkyl, alkoxy, haloalkyl,and haloalkoxy; or R⁵ and R⁶ together form a fused cycloalkyl orheterocycloalkyl ring having from 5 to 6 ring atoms selected from thegroup consisting of carbon, nitrogen, and oxygen; and

E is selected from the group consisting of S, O, N(H), N(CH₃), and CH₂.

Alternatively, the compound of Formula II may be a compound of FormulaIIb or a salt thereof,

wherein

R¹ is a prodrug of carboxylic acid;

R² is selected from the group consisting of alkyl, cycloalkyl,heterocycloalkyl, aryl and heteroaryl, each of which may be optionallyindependently substituted with one or more substituents selected fromthe group consisting of halogen, CH₃, OCH₃, CF₃, OCF₃, and CN;

R³ is selected from the group consisting of hydrogen, CN, ethynyl,CH₂N(R⁹R¹⁰), and C(O)N(R⁹R¹⁰), wherein R⁹ and R¹⁰ are each independentlyselected from the group consisting of hydrogen and alkyl;

R⁴ is selected from the group consisting of haloalkyl, aryl, arylalkyl,heteroaryl, and heteroarylalkyl, each of which may be optionallyindependently substituted with one or more substitutents selected fromthe group consisting of halogen, alkyl, alkoxy, haloalkyl, haloalkoxy,alkenyl, hydroxyalky, hydroxy, N(R⁹R¹⁰), NR¹¹C(O)R¹² and O(CO)R¹³,wherein R⁹ and R¹⁰ are independently selected from the group consistingof hydrogen and alkyl, R¹¹ is selected from the group consisting ofhydrogen and alkyl, R¹² is alkyl, and R¹³ is alkyl;

R⁵ is selected from the group consisting of hydrogen or alkyl; or R⁴ andR⁵ together form a fused cycloalkyl or heterocycloalkyl ring having from5 to 6 ring atoms selected from the group consisting of carbon,nitrogen, and oxygen;

R⁶ is selected from the group consisting of alkyl, haloalkyl, aryl,arylalkyl, heteroaryl, and heteroarylalkyl, each of which may beoptionally independently substituted with one or more substitutentsselected from the group consisting of halogen, alkyl, alkoxy, haloalkyl,and haloalkoxy; or R⁵ and R⁶ together form a fused cycloalkyl orheterocycloalkyl ring having from 5 to 6 ring atoms selected from thegroup consisting of carbon, nitrogen, and oxygen; and

E is selected from the group consisting of S, O, N(H), N(CH₃), and CH₂.

In some embodiments, the compound is a compound of Formula II, IIa, orIIb wherein R² is phenyl.

In some embodiments, the compound is a compound of Formula II, IIa, orIIb wherein R³ is CN.

In some embodiments, the compound is a compound of Formula II, IIa, orIIb wherein R⁴ is selected from the group consisting of CF₃, thienyl,and optionally substituted phenyl. For example, R⁴ may be 4-halophenyl(e.g., 4-chlorophenyl) or 4-alkoxyphenyl (e.g., 4-methoxyphenyl).

In some embodiments, the compound is a compound of Formula II, IIa, orIIb wherein R⁵ is hydrogen.

In some embodiments, the compound is a compound of Formula II, IIa, orIIb wherein R⁶ is selected from the group consisting of methyl, ethyl,thienyl, furanyl, and optionally substituted phenyl. In one embodiment,R⁶ may be 4-halophenyl (e.g., 4-bromophenyl) or 4-alkoxyphenyl (e.g.,4-methoxyphenyl). In some embodiments, R⁶ may be disubstituted phenyl(e.g., 2,4-disubstituted phenyl or 3,4-disubstituted phenyl). In otherembodiments, R⁶ may be 2,4-dimethoxyphenyl or 3,4-dimethoxyphenyl.

In some embodiments, the compound is a compound of Formula II, IIa, orIIb wherein E is selected from the group consisting of S, O, and CH₂. Inother embodiments, E may be S.

In some embodiments, the compound is a compound of Formula II or IIawherein R¹ is a carboxylic acid isostere selected from the groupconsisting of tetrazolyl, aminosulfonyl, acylaminosulfonyl,methylsulfonylcarbamyl, thiazolidinedionyl, oxazolidinedionyl,oxadiazolonyl, P(O)(OH)₂, P(O)(OH)H, and SO₃H.

In some embodiments, the compound is a compound of Formula II or IIbwherein R¹ is a prodrug of carboxylic acid selected from the groupconsisting of CH₂OH and ester group C(O)OR¹⁴, wherein R¹⁴ is selectedfrom the group consisting of methyl, ethyl, 2-oxopropyl,2-morpholinoethyl, and pivaloyloxymethyl. For example, in someembodiments, R¹ is C(O)OCH₃. In other embodiments, R¹ is CH₂OH.

As used herein, the term “halo” or “halogen” refers to any radical offluorine, chlorine, bromine or iodine.

The term “alkyl” as employed herein, by itself or as part of anothergroup, refers to both straight and branched chain radicals of up to tencarbons, which may be optionally independently substituted. Non-limitingexamples of C₁-C₁₀ alkyl groups include methyl, ethyl, propyl,isopropyl, butyl, sec-butyl, tert-butyl, 3-pentyl, hexyl and octylgroups. For example, in some embodiments, the term “alkyl” as usedherein, by itself or as part of another group, refers to a straight orbranched chain radical comprising from one to six carbon atoms.

The term “hydroxyalkyl” as employed herein, refers to both straight andbranched chain alkyl radicals having a hydroxyl substituent. Thehydroxyl substituent can be bound to any carbon of the alkyl chain.Non-limiting examples include CH₂OH, CH₂CH₂OH, CH₂CH(OH)CH₃ andCH₂CH(OH)CH₂CH₃. For example, in some embodiments, the term“hydroxyalkyl” as employed herein refers to a straight or branched chainradical comprising from one to four carbon atoms and having one or morehydroxyl substituents.

The term “haloalkyl” as employed herein, by itself or as part of anothergroup, refers to an alkyl group, as defined herein, substituted with atleast one halogen. Non-limiting examples of haloalkyl groups includetrifluromethyl and 2,2,2-trifluoroethyl.

The term “alkoxy” as employed herein, by itself or as part of anothergroup, refers to an alkyl group, as defined herein, appended to theparent molecular moiety through an oxygen atom. Non-limiting examples ofalkoxy groups include methoxy, ethoxy, propoxy, 2-propoxy, butoxy,tert-butoxy, pentyloxy, and hexyloxy.

The term “haloalkoxy” as employed herein, by itself or as part ofanother group, refers to an alkoxy group as defined herein, wherein thealkyl moiety of the alkoxy group is further substituted with at leastone halogen. Non-limiting example of haloalkoxy groups includetrifluoromethoxy, and 2,2-dichloroethoxy.

The term “cycloalkyl” as used herein refers to an alkyl group comprisinga closed ring comprising from 3 to 8 carbon atoms. Non-limiting examplesof cycloalkyl groups include cyclopropyl, cyclobutyl, cyclopentyl,cyclohexyl and cycloheptyl.

As used herein, the term “heterocyclyl,” “heterocycloalkyl,” or“heterocycle” refers to a saturated or partially saturated 3 to 7membered monocyclic, or 7 to 10 membered bicyclic ring system, whichconsists of carbon atoms and from one to four heteroatoms independentlyselected from the group consisting of O, N, and S, wherein the nitrogenand sulfur heteroatoms can be optionally oxidized, the nitrogen can beoptionally quaternized, and includes any bicyclic group in which any ofthe above-defined heterocyclic rings is fused to a benzene ring, andwherein the heterocyclic ring can be substituted on carbon or on anitrogen atom if the resulting compound is stable. Non-limiting examplesof common saturated or partially saturated heterocyclic groups includetetrahydrofuranyl, pyranyl, piperidinyl, piperazinyl, pyrrolidinyl,imidazolidinyl, imidazolinyl, indolinyl, isoindolinyl, quinuclidinyl,morpholinyl, isochromanyl, chromanyl, pyrazolidinyl pyrazolinyl,tetronoyl and tetramoyl groups.

The term “aryl” as employed herein by itself or as part of another grouprefers to monocyclic, bicyclic or tricyclic aromatic groups containingfrom 6 to 14 carbons in the ring. Common aryl groups include C₆₋₁₄ aryl,preferably C₆₋₁₀ aryl. Typical C₆₋₁₄ aryl groups include phenyl,naphthyl, phenanthrenyl, anthracenyl, indenyl, azulenyl, biphenyl,biphenylenyl and fluorenyl groups.

The term “heteroaryl” as employed herein refers to groups having 5 to 14ring atoms; 6, 10 or 14 π electrons shared in a cyclic array; andcontaining carbon atoms and 1, 2 or 3 oxygen, nitrogen or sulfurheteroactoms. Example heteroaryl groups include thienyl(thiophenyl),benzo[b]thienyl, naphtho[2,3-b]thienyl, thianthrenyl, furyl(furanyl),pyranyl, isobenzofuranyl, chromenyl, xanthenyl, phenoxanthiinyl,pyrrolyl, including without limitation 2H-pyrrolyl, imidazolyl,pyrazolyl, pyridyl(pyridinyl), including without limitation 2-pyridyl,3-pyridyl, and 4-pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl,indolizinyl, isoindolyl, 3H-indolyl, indolyl, indazolyl, purinyl,4H-quinolizinyl, isoquinolyl, quinolyl, phthalzinyl, naphthyridinyl,quinozalinyl, cinnolinyl, pteridinyl, carbazolyl, β-carbolinyl,phenanthridinyl, acrindinyl, perimidinyl, phenanthrolinyl, phenazinyl,isothiazolyl, phenothiazinyl, isoxazolyl, furazanyl, phenoxazinyl,1,4-dihydroquinoxaline-2,3-dione, 7-aminoisocoumarin,pyrido[1,2-α]pyrimidin-4-one, pyrazolo[1,5-α]pyrimidinyl, includingwithout limitation pyrazolo[1,5-α]pyrimidin-3-yl,1,2-benzoisoxazol-3-yl, benzimidazolyl, 2-oxindolyl and2-oxobenzimidazolyl. Where the heteroaryl group contains a nitrogen atomin a ring, such nitrogen atom may be in the form of an N-oxide, e.g., apyridyl N-oxide, pyrazinyl N-oxide and pyrimidinyl N-oxide.

The term “prodrug of a carboxylic acid” as employed herein refers to anycompound or moiety that can be transformed through chemical or metabolic(enzymatic) processes in vivo to produce carboxylic acid. The prodrug ofa carboxylic acid may be an inactive or less active compound than theparent compound containing the carboxylic acid. A prodrug of acarboxylic acid may have physicochemical properties which result inimproved uptake, distribution or metabolism. In a non-limiting exampleof a prodrug of a carboxylic acid, the carboxylic acid can be esterifiedwith a methyl or ethyl group to yield an ester and when the carboxylicacid ester is administered to a biological system (e.g. plant or humansubject) the ester group may be, for example, converted enzymatically,non-enzymatically, oxidatively or hydrolytically to the carboxylategroup. Additionally, cleavable carboxylic acid prodrug moieties include,but are not limited to, substituted and unsubstituted, branched andunbranched lower alkyl ester moieties (methyl ester, ethyl esters,propyl esters, butyl esters, pentyl esters, cyclopentyl esters, hexylesters and cyclohexyl esters), lower alkenyl esters, acyloxy lower alkylesters (e.g. pivaloyloxymethyl ester), aryl esters, and aryl lower alkylesters (e.g. benzyl esters). Alternatively, hydroxyalkyl groups may beoxidized in vivo to a carboxylic acid. Additionally, conventionalprocedures for selection and preparation of suitable prodrug of acarboxylic acid derivatives are known in the art including, for example,as described in “Prodrugs: Challenges and Rewards”, Part 2, Volume 5(2007) pages 3-29 and “Current Methods in Medicinal Chemistry andBiological Physics” Volume 2 (2008) pages 187-214”, which areincorporated herein by reference.

The term “carboxylic acid isostere” as employed herein includes each andall of (1) carboxylic acid isosteres having one or more of thefollowing, the same number of atoms, the same number of valenceelectrons, and exhibiting similar reactive electron shells, volumes andshapes as compared to a carboxylic acid substituent, and (2)non-classical isosteres which fit the broadest definition of isostersand produce biological effects similar to a carboxylic acid substituent.Non-limiting examples of carboxylic acid isosteres include tetrazolyl,aminosulfonyl, acylaminosulfonyl, methyl sulfonyl carbamyl,thiazolidinedionyl, oxazolidinedionyl, oxadiazolonyl, P(O)(OH)₂,P(O)(OH)H, and SO₃H. The concept of carboxylic acid isostere in drugdesign and the properties of several isosters are known in the art anddescribed, for example, by Ballatore at al in ChemMedChem 2013, 8, pages385-395, which is incorporated herein by reference.

Non-limiting examples of species include2-((4-(4-chlorophenyl)-3-cyano-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid of Formula Ia-i, or a salt thereof,

2-((3-cyano-6-(thiophen-2-yl)-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylaceticacid of Formula Ia-ii, or a salt thereof,

2-((3-cyano-4,6-di(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetic acidof Formula Ia-iii, or a salt thereof,

2-((3-cyano-4-phenyl-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid of Formula Ia-iv, or a salt thereof,

2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid of Formula Ia-v, or a salt thereof,+

2-((3-cyano-8-methyl-4-(thiophen-2-yl)-5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)thio)-2-phenylaceticacid of Formula Ia-vi, or a salt thereof,

2-((4-cyano-1-(thiophen-2-yl)-5,6,7,8-tetrahydroisoquinolin-3-yl)thio)-2-phenylaceticacid of Formula Ia-vii, or a salt thereof,

2-((3-cyano-6-(2,4-dimethoxyphenyl)-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylaceticacid of Formula Ia-viii, or a salt thereof,

2-((3-cyano-6-(3,4-dimethoxyphenyl)-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylaceticacid of Formula Ia-ix, or a salt thereof,

2-((6-(4-bromophenyl)-3-cyano-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylaceticacid of Formula Ia-x, or a salt thereof,

2-((3-cyano-6-(furan-2-yl)-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylaceticacid of Formula Ia-xi, or a salt thereof,

2-((3-cyano-4,6-diphenylpyridin-2-yl)thio)-2-phenylacetic acid ofFormula Ia-xii, or a salt thereof,

2-((3-cyano-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylaceticacid of Formula Ia-xiii, or a salt thereof,

2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid of Formula Ia-xiv, or a salt thereof,

2-((4-cyano-1-ethyl-5,6,7,8-tetrahydroisoquinolin-3-yl)thio)-2-phenylaceticacid of Formula Ia-xv, or a salt thereof,

2-((3-cyano-6-methyl-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylaceticacid of Formula Ia-xvi, or a salt thereof,

2-((3-cyano-4-phenyl-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylaceticacid of Formula Ia-xvii, or a salt thereof,

2-((4-(4-chlorophenyl)-3-cyano-5,6,7,8-tetrahydronaphthalen-2-yl)thio)-2-phenylaceticacid of Formula Ia-xviii, or a salt thereof,

2-((4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid of Formula Ia-xix, or a salt thereof,

2-((3-cyano-6-(furan-2-yl)-4-(4-methoxyphenyl)pyridin-2-yl)thio)-2-phenylaceticacid of Formula Ia-xx, or a salt thereof,

2-((3-cyano-6-(thiophen-2-yl)-4-(p-tolyl)pyridin-2-yl)thio)-2-phenylaceticacid of Formula Ia-xxi, or a salt thereof,

2-((3-cyano-4-(4-fluorophenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid of Formula Ia-xxii, or a salt thereof,

2-((4-(4-bromophenyl)-3-cyano-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid of Formula Ia-xxiii, or a salt thereof,

2-((3-cyano-6-(furan-2-yl)-4-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid of Formula Ia-xxiv, or a salt thereof,

2-((3-cyano-4,6-di(furan-2-yl)pyridin-2-yl)thio)-2-phenylacetic acid ofFormula Ia-xxv, or a salt thereof,

2-((3-cyano-4-(4-methoxyphenyl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylaceticacid of Formula Ia-xxvi, or a salt thereof

2-((3-cyano-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinolin-2-yl)oxy)-2-phenylaceticacid of Formula Ia-xxvii, or a salt thereof,

2-((3-cyano-4-(4-methoxyphenyl)-6-(1-oxidothiophen-2-yl)pyridin-2-yl)oxy)-2-phenylaceticacid of Formula Ia-xxviii, or a salt thereof,

2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)butanoicacid of Formula Ia-xxix, or a salt thereof,

2-((3-cyano-4-(4-methoxyphenyl)-6-(pyrimidin-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid of Formula Ia-xxx, or a salt thereof

2-((3-cyano-6-(3-methoxy-1-methyl-1H-pyrrol-2-yl)-4-(4-methoxyphenyl)pyridin-2-yl)thio)-2-phenylaceticacid of Formula Ia-xxxi, or a salt thereof,

2-((3-cyano-4-(furan-2-yl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid of Formula Ia-xxxii, or a salt thereof,

2-((3-cyano-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylacetamideof Formula Ib-i, or a salt thereof,

2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetamideof Formula Ib-ii, or a salt thereof,

2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-N-hydroxy-2-phenylacetamideof Formula Ib-iii, or a salt thereof,

4-(4-methoxyphenyl)-2-((phenyl(1H-tetrazol-5-yl)methyl)thio)-6-(thiophen-2-yl)nicotinonitrileof Formula IIa-i, or a salt thereof,

(((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)(phenyl)methyl)phosphonicacid of Formula IIa-ii, or a salt thereof,

(((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)(phenyl)methyl)phosphinicacid of Formula IIa-iii, or a salt thereof,

((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)(phenyl)methanesulfonicacid of Formula IIa-iv, or a salt thereof,

((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)(phenyl)methanesulfonamideof Formula IIa-v, or a salt thereof,

2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-N-(methylsulfonyl)-2-phenylacetamideof Formula IIa-vi, or a salt thereof,

2-(((2,4-dioxothiazolidin-5-yl)(phenyl)methyl)thio)-4-(4-methoxyphenyl)-6-(thiophen-2-yl)nicotinonitrileof Formula IIa-vii, or a salt thereof,

2-(((2,4-dioxooxazolidin-5-yl)(phenyl)methyl)thio)-4-(4-methoxyphenyl)-6-(thiophen-2-yl)nicotinonitrileof Formula IIa-viii, or a salt thereof,

4-(4-methoxyphenyl)-2-(((5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)(phenyl)methyl)thio)-6-(thiophen-2-yl)nicotinonitrileof Formula IIa-ix, or a salt thereof,

2-((2-hydroxy-1-phenylethyl)thio)-4-(4-methoxyphenyl)-6-(thiophen-2-yl)nicotinonitrileof Formula IIb-i, or a salt thereof,

2-((2-hydroxy-1-phenylethyl)thio)-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinoline-3-carbonitrileof Formula IIb-ii, or a salt thereof,

methyl2-((3-cyano-6-(thiophen-2-yl)-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylacetateof Formula IIb-iii, or a salt thereof, and

4-(furan-2-yl)-2-(((2-hydroxy-1-phenylethyl)thio)-6-(thiophen-2-yl)nicotinonitrileof Formula IIb-iv, or a salt thereof.

Enantiomers

The compounds described herein can be present as a racemic mixture, as amixture of two enantiomers at different ratios, or as a singleenantiomer. Compositions that are enriched with respect to oneenantiomer, or which comprise substantially a single enantiomer, may beprepared using any technique known in the art, including chiralseparation techniques known in the art (e.g., chiral chromatography orasymmetric synthesis).

Compositions

In another aspect, the present disclosure is generally related to acomposition comprising an effective amount of a compound (e.g., acompound of Formula I, Ia, Ib, II, IIa, or IIb) as described herein asan ACCase modulator or inhibitor for use in administration to a plant, aseed, or soil to control fungal pathogens.

For example, the composition may be an aqueous composition.

Generally, compositions described herein can comprise any adjuvants,excipients, or other desirable components known in the art.

Non-limiting examples of additional ingredients include surfactants,co-surfactants, permeation enhancers, and co-solvents. For example, thecomposition may comprise as SPAN surfactants, TWEEN surfactants, TRITONsurfactants, MAKON surfactants, IGEPAL surfactants, BRIJ surfactants,MORWET surfactants, PLURONIC surfactants, LANEXOL surfactants, ATLOXsurfactants, ATLAS surfactants, SURFYNOL surfactants, TERGITOLsurfactants, DOWFAX surfactants, TOXIMUL surfactants, SILWETsurfactants, SYLGARD surfactants, BREAK THRU surfactants, PHYTOSAN,SOLUPLUS, cyclodextrans, polypropylene glycol, ethyl lactate, methylsoyate/ethyl lactate co-solvent blends (e.g., STEPOSOL), isopropanol,acetone, ethylene glycol, propylene glycol, n-alkylpyrrolidones (e.g.,the AGSOLEX series), a petroleum based-oil (e.g., AROMATIC 200) or amineral oil (e.g., paraffin oil)).

For example, in some embodiments, a composition comprises a surfactant.Non-limiting examples of surfactants include SPAN 20, SPAN 40, SPAN 80,SPAN 85, TWEEN 20, TWEEN 40, TWEEN 80, TWEEN 85, TRITON X 100, MAKON 10,IGEPAL CO 630, BRIJ 35, BRIJ 97, TERGITOL TMN 6, DOWFAX 3B2, PHYSAN andTOXIMUL TA 15.

In some embodiments, a composition comprises a co-solvent. Examples ofco-solvents that can be used include ethyl lactate, methyl soyate/ethyllactate co-solvent blends (e.g., STEPOSOL), isopropanol, acetone,1,2-propanediol, n-alkylpyrrolidones (e.g., the AGSOLEX series), apetroleum based-oil (e.g., AROMATIC 200) or a mineral oil (e.g.,paraffin oil)).

In some embodiments, a composition may be formulated, mixed in a tank,combined on a seed by overcoating, or recommended for use with one ormore additional active ingredients on a seed, plant, or soil. Theadditional active ingredient may be, for example, an additionalpesticide. The pesticide may be, for example, an insecticide, afungicide, an herbicide, or an additional nematicide.

Non-limiting examples of insecticides and nematicides includecarbamates, diamides, macrocyclic lactones, neonicotinoids,organophosphates, phenylpyrazoles, pyrethrins, spinosyns, syntheticpyrethroids, tetronic and tetramic acids. In another embodiment,insecticides and nematicides include abamectin, aldicarb, aldoxycarb,bifenthrin, carbofuran, chlorantraniliprole, clothianidin, cyfluthrin,cyhalothrin, cypermethrin, deltamethrin, dinotefuran, emamectin,ethiprole, fenamiphos, fipronil, flubendiamide, fosthiazate,imidacloprid, ivermectin, lambda-cyhalothrin, milbemectin, nitenpyram,oxamyl, permethrin, spinetoram, spinosad, spirodichlofen, spirotetramat,tefluthrin, thiacloprid, thiamethoxam, and thiodicarb.

In some embodiments, a composition comprises an insecticide and/oracaricide that inhibits ACCase activity. Non-limiting examples includetetramic acids such as spirotetramat, and tetronic acids includingspiromesifen and spirodiclofen.

In some embodiments, the composition comprises one or more nematicidalcompounds as described in U.S. Pub. Nos. 2009/0048311 A1 or 2011/028320A1, or WO 2012/030887 A1, the contents of which are herein incorporatedby reference.

For example, in some embodiments, the composition comprises3-phenyl-5-(thiophen-2-yl)-1,2,4-oxadiazole.

Non-limiting examples of herbicides include ACCase inhibitors,acetanilides, AHAS modulators or inhibitors, carotenoid biosynthesisinhibitors, EPSPS modulators or inhibitors, glutamine synthetasemodulators or inhibitors, PPO modulators or inhibitors, PS II modulatorsor inhibitors, and synthetic auxins. Non-limiting examples of herbicidesinclude acetochlor, clethodim, dicamba, flumioxazin, fomesafen,glyphosate, glufosinate, mesotrione, quizalofop, saflufenacil,sulcotrione, and 2,4-D.

In one embodiment, an herbicide is selected that inhibits ACCaseactivity. Non-limiting examples include herbicidalaryloxyphenoxypropionates such as chlorazifop, clodinafop, clofop,cyhalofop, diclofop, fenoxaprop, fenoxaprop-P, fenthiaprop, fluazifop,fluazifop-P, haloxyfop, haloxyfop-P, isoxapyrifop, kuicaoxi, metamifop,propaquizafop, quizalofop, quizalofop-P, and trifop, herbicidalcyclohexanediones such as alloxydim, butroxydim, clethodim, cloproxydim,cycloxydim, profoxydim, sethoxydim, tepraloxydim, and tralkoxydim, aswell as the herbicide pinoxaden.

The herbicides cycloxydim and sethoxydim are known to exhibit moderateantifungal activity alone, and, without being bound to a particulartheory, it is believed that the combination of these species with thecompounds described herein may enhance fungal control by the additionalsuppression of ACCase.

A composition may comprise one or more additional fungicides.Non-limiting examples of additional fungicides include aromatichydrocarbons, benzimidazoles, benzothiadiazole, carboxamides, carboxylicacid amides, morpholines, phenylamides, phosphonates, quinine outsideinhibitors (e.g. strobilurins), thiazolidines, thiophanates, thiophenecarboxamides, and triazoles, Particular examples of fungicides includeacibenzolar-S-methyl, azoxystrobin, benalaxyl, bixafen, boscalid,carbendazim, cyproconazole, dimethomorph, epoxiconazole, fluopyram,fluoxastrobin, flutianil, flutolanil, fluxapyroxad, fosetyl-A1,ipconazole, isopyrazam, kresoxim-methyl, mefenoxam, metalaxyl,metconazole, myclobutanil, orysastrobin, penflufen, penthiopyrad,picoxystrobin, propiconazole, prothioconazole, pyraclostrobin, sedaxane,silthiofam, tebuconazole, thifluzamide, thiophanate, tolclofos-methyl,trifloxystrobin, and triticonazole.

In some embodiments, the composition comprises one or more additionalfungicides that modulate or inhibit ACCase activity.

A composition may also comprise one or more additional activesubstances, including biological control agents, microbial extracts,natural products, plant growth activators and/or plant defense agents.Non-limiting examples of biological control agents include bacteria,fungi, beneficial nematodes, and viruses.

For example, in certain embodiments, the biological control agent can bea bacterium of the genus Actinomycetes, Agrobacterium, Arthrobacter,Alcaligenes, Aureobacterium, Azobacter, Beijerinckia, Brevibacillus,Burkholderia, Chromobacterium, Clostridium, Clavibacter, Comamonas,Corynebacterium, Curtobacterium, Enterobacter, Flavobacterium,Gluconobacter, Hydrogenophage, Klebsiella, Methylobacterium,Paenibacillus, Pasteuria, Photorhabdus, Phyllobacterium, Pseudomonas,Rhizobium, Serratia, Sphingobacterium, Stenotrophomonas, Variovax, andXenorhabdus.

In some embodiments, the biological control agent can be a fungus of thegenus Alternaria, Ampelomyces, Aspergillus, Aureobasidium, Beauveria,Colletotrichum, Coniothyrium, Gliocladium, Metarhizium, Muscodor,Paecilomyces, Trichoderma, Typhula, Ulocladium, and Verticillium. Inparticular embodiments the fungus is Beauveria bassiana, Coniothyriumminitans, Gliocladium virens, Muscodor albus, Paecilomyces lilacinus, orTrichoderma polysporum.

In further embodiments, the biological control agents can be plantgrowth activators or plant defense agents including, but not limited toharpin, Reynoutria sachalinensis, jasmonate, lipochitooligosaccharides,and isoflavones.

Methods of Use

ACCase is an essential catalyst for the rate-limiting step of fatty acidbiosynthesis in both eukaryotes and prokaryotes. Without being bound toa particular theory, it is believed that the compounds disclosed hereinmodulate or inhibit ACCase. In one embodiment, a compound (e.g., acompound of Formula I, Ia, Ib, II, IIa, or IIb) as described herein isused as a ACCase modulator. Additionally, compounds as described hereinof Formulas I, Ia, Ib, II, IIa, and IIb are also believed to exhibitcontrol of phytopathogenic fungi as described herein. In one embodiment,the compounds disclosed herein are administered to a plant, a seed, orsoil in a composition as described herein to control fungal pathogens,including using the compounds as described herein with any adjuvants,excipients, or other desirable components as described herein or knownin the art and formulating, mixing, or combining one or more additionalactive ingredients. The additional active ingredient may be, forexample, an additional pesticide. The pesticide may be, for example, aninsecticide, a fungicide, an herbicide, or an additional nematicide asdescribed herein or otherwise known in the art.

Compounds and compositions described herein can be administered toseeds, plants, or the environment of plants (e.g., soil) wherein thecontrol of phytopathogenic fungi is desired. For example, in oneembodiment, the disclosure is generally related to a method ofcontrolling fungal pathogens, the method comprising administering to aplant, a seed or soil a composition comprising an effective amount of acompound as described herein.

Non-limiting examples of plants that may be protected from fungalpathogens in accordance with the methods described herein includemonocotyledon crops such as corn, wheat, barley, rye, rice, sorghum,oat; sugarcane and turf; and dicotyledon crops such as cotton, sugarbeet, peanut, potato, sweet potato, yam, sunflower, soybean, alfalfa,canola, grapes, tobacco; vegetables including Solanaceae vegetables suchas eggplant, tomato, green pepper and pepper; Cucurbitaceae vegetablessuch as cucumber, pumpkin, zucchini, watermelon, melon and squash;Brassicaceae vegetables such as radish, turnip, horseradish, Chinesecabbage, cabbage, leaf mustard, broccoli and cauliflower; Asteraceaevegetables such as artichoke and lettuce; Liliaceae vegetables such asleek, onion, garlic and asparagus; Apiaceae vegetables such as carrot,parsley, celery and parsnip; Chenopodiaceae vegetables such as spinachand chard; Lamiaceae vegetables such as mint and basil; flowers such aspetunia, morning glory, carnation, chrysanthemum and rose; foliageplants; fruit trees such as pome fruits (e.g., apple, pear and Japanesepear), stone fruits (e.g., peach, plum, nectarine, cherry, apricot andprune), citrus (e.g., orange, lemon, lime and grapefruit), tree nuts(e.g., chestnut, pecan, walnut, hazel, almond, pistachio, cashew andmacadamia), berries such as blueberry, cranberry, blackberry, strawberryand raspberry; persimmon; olive; loquat; banana; coffee; palm; coco; theother trees such tea, mulberry, flower trees, and landscape trees (e.g.,ash, birch, dogwood, eucalyptus, ginkgo, lilac, maple, oak, poplar,Formosa sweetgum, sycamore, fir, hemlock fir, needle juniper, pine,spruce, yew).

Non-limiting examples of the plant diseases that may be controlled bythe methods described herein include diseases caused by phytopathogenicfungi (in particular of the classes of Ascomycetes, Deuteromycetes,Oomycetes and Basidiomycetes) such as Magnaporthe grisea, Cochliobolusmiyabeanus, Rhizoctonia solani and Gibberella fujikuroi on rice;Erysiphe graminis, Fusarium graminearum, F. avenacerum, F. culmorum,Microdochium nivale, Puccinia striiformis, P. graminis, P. recondita, P.hordei, Typhula sp., Micronectriella nivalis, Ustilago tritici, U. nuda,Tilletia caries, Pseudocercosporella herpotrichoides, Rhynchosporiumsecalis, Septoria tritici, Leptosphaeria nodorum and Pyrenophora tereson wheat and barley; Diaporthe citri, Elsinoe fawcetti, Penicilliumdigitatum, P. italicum, Phytophthora parasitica and Phytophthoracitrophthora on citrus; Monilinia mali, Valsa ceratosperma, Podosphaeraleucotricha, Alternaria alternata apple pathotype, Venturia inaequalis,Colletotrichum acutatum and Phytophtora cactorum on apple; Venturianashicola, V. pirina, Alternaria alternata Japanese pear pathotype,Gymnosporangium haraeanum and Phytophthora cactorum on pear; Moniliniafructicola, Cladosporium carpophilum and Phomopsis sp. on peach; Elsinoeampelina, Glomerella cingulata, Uncinula necator, Phakopsoraampelopsidis, Guignardia bidwellii and Plasmopara viticola on grape;Gloeosporium kaki, Cercospora kaki and Mycosphaerella nawae onpersimmon; Colletotrichum lagenarium, Sphaerotheca fuliginea,Mycosphaerella melonis, Fusarium oxysporum, Pseudoperonospora cubensisand Phytophthora sp. on Cucurbitales vegetables; Alternaria solani,Cladosporium fulvum and Phytophthora infestans on tomato; Phomopsisvexans and Erysiphe cichoracearum on eggplant; Alternaria japonica,Cercosporella brassicae, Plasmodiophora brassicae and Peronosporaparasitica on Brassicaceae vegetables; Puccinia allii and Peronosporadestructor on leek; Cercospora kikuchii, Elsinoe glycines, Diaporthephaseolorum var. sojae, Phakopsora pachyrhizi and Phytophthora sojae onsoybean; Colletotrichum lindemuthianum of kidney bean; Cercosporapersonata, Cercospora arachidicola and Sclerotium rolfsii on peanut;Erysiphe pisi on pea; Alternaria solani, Phytophthora infestans,Phytophthora erythroseptica and Spongospora subterranean f. sp.subterranean on potato; Sphaerotheca humuli and Glomerella cingulata onstrawberry; Exobasidium reticulatum, Elsinoe leucospila, Pestalotiopsissp. and Colletotrichum theae-sinensis on tea; Alternaria longipes,Erysiphe cichoracearum, Colletotrichum tabacum, Peronospora tabacina andPhytophthora nicotianae on tobacco; Cercospora beticola, Thanatephoruscucumeris, and Aphanidermatum cochlioides on sugar beet; Diplocarponrosae, Sphaerotheca pannosa and Peronospora sparsa on rose; Bremialactucae, Septoria chrysanthemi-indici and Puccinia horiana onchrysanthemum and Compositae vegetables; Alternaria brassicicola onradish; Sclerotinia homeocarpa and Rhizoctonia solani on turf;Mycosphaerella fijiensis and Mycosphaerella musicola on banana;Plasmopara halstedii on sunflower; and various diseases on crops causedby Aspergillus spp., Alternaria spp., Cephalosporium spp., Cercosporaspp., Cochliobolus spp., Diaporthe spp., Phomopsis spp., Diplodia spp.,Fusarium spp., Gibberella spp., Helminthosporium spp., Phakopsora spp.,Phytophthora spp., Blumeria spp., Oidium spp., Erysiphe spp., Uncinulaspp., Podosphaera spp., Microsphaera spp., Colletotrichum spp.,Corynespora spp., Peronospora spp., Plasmopara spp., Pythium spp.,Pyrenophora spp., Pythium spp., Rhizoctonia spp., Rhynchosporium spp.,Botryotinia spp., Botrytis spp., Botryosphaeria spp., Sphaerotheca spp.,Septoria spp., Thielaviopsis spp., Typhula spp., Pseudocercosporellaspp., Cochliobolus spp., Gaeumannomyces spp., Mucor spp., Puccinia spp.,Tilletia spp., Ustilago spp., Venturia spp., Gymnosporangium spp.,Claviceps spp., Cladosporium spp., Physalospora spp., Pyricularia spp.,Magnaporthe spp., Rhizopus spp., Monilinia spp., Cladosporium spp.,Curvularia spp., Sclerotinia spp., Sclerotium sp., Corticum spp.,Corticium spp., Phoma spp., Polymyxa spp., and Olpidium spp.

Application to Plants and/or Soil

Generally, the methods described herein can be used to modulate, inhibitor eradicate fungal pathogens as described herein that cause disease onvarious parts of agricultural crop plants (e.g., fruit, blossoms,leaves, stems, tubers, roots) or other useful plants as describedherein. For example, the methods described herein may be used tomodulate, inhibit, and/or control any of the fungal pathogens and/orplant diseases listed above.

For example, methods described herein may be used to modulate, inhibitor eradicate plant fungal pathogens in vegetable crops, row crops,trees, nuts, vines, turf, and ornamental plants.

In some embodiments, a composition comprising a compound as describedherein may be supplied to a plant exogenously. The composition may beapplied to the plant and/or the surrounding soil through sprays, drips,and/or other forms of liquid application.

The compounds described herein may penetrate the plant through the rootsvia the soil (systemic action); by drenching the locus of the plant witha liquid composition; or by applying the compounds in solid form to thesoil, e.g. in granular form (soil application).

As used herein, the term “locus” broadly encompasses the fields on whichthe treated plants are growing, or where the seeds of cultivated plantsare sown, or the place where the seed will be placed into the soil.

For example, in some embodiments, a composition is applied to a plant,including plant leaves, shoots, roots, or seeds. In one embodiment, acomposition comprising a compound as described herein applied to afoliar surface of a plant. Foliar applications may require 50 to 500 gper hectare of a compound as described herein.

As used herein, the term “foliar surface” broadly refers to any greenportion of a plant having surface that may permit absorption of silicon,including petioles, stipules, stems, bracts, flowerbuds, and leaves.Absorption commonly occurs at the site of application on a foliarsurface, but in some cases, the applied composition may run down toother areas and be absorbed there.

Compositions described herein can be applied to the foliar surfaces ofthe plant using any conventional system for applying liquids to a foliarsurface. For example, in some embodiments, application by spraying willbe found most convenient. Any conventional atomization method can beused to generate spray droplets, including hydraulic nozzles androtating disk atomizers. In some embodiments, alternative applicationtechniques, including application by brush or by rope-wick, may beutilized.

In some embodiments, a composition comprising a compound as describedherein is directly applied to the soil surrounding the root zone of aplant. Soil applications may require 0.5 to 5 kg per hectare of acompound as described herein on a broadcast basis (rate per treated areaif broadcast or banded).

For example, in some embodiments, a composition may be applied directlyto the base of the plants or to the soil immediately adjacent to theplants.

In some embodiments, a sufficient quantity of the composition is appliedsuch that it drains through the soil to the root area of the plants.

Generally, application of a composition may be performed using anymethod or apparatus known in the art, including but not limited to handsprayer, mechanical sprinkler, or irrigation, including drip irrigation.

In some embodiments, a composition is applied to plants and/or soilusing a drip irrigation technique. For example, the composition may beapplied through existing drip irrigation systems. This procedure is usedin some embodiments in connection with cotton, strawberries, tomatoes,potatoes, vegetables, and ornamental plants.

In other embodiments, a composition is applied to plants and/or soilusing a drench application. The drench application technique is used insome embodiments in connection with crop plants and turf grasses.

In some embodiments, a composition is applied to soil after planting. Inother embodiments, however, a composition may be applied to soil duringplanting, or a composition may be applied to soil before planting.

For example, in some embodiments, a composition may be tilled into thesoil or applied in furrow.

In crops of water, such as rice, solid granulates comprising thecompounds described herein may be applied to the flooded field or locusof the crop plants to be treated.

Application to Seeds

One embodiment of the disclosure is generally related to a method ofprotecting a seed, and/or the roots of a plant grown from the seed,against damage by phytopathogenic fungi. The seed treatment methodsdescribed herein may be used to modulate, inhibit, and/or control any ofthe fungal pathogens and/or plant diseases described above. In oneembodiment, the method comprises treating a seed with a compositioncomprising a compound as described herein. As used herein, the term“seed” broadly encompasses plant propagating material such as, tuberscuttings, seedlings, seeds, and germinated or soaked seeds.

In one embodiment, the disclosure relates to a method of administeringto a seed a compound (e.g., a compound of Formula I, Ia, Ib, II, IIa, orIIb) as described to control fungal pathogens in a composition asdescribed herein, including using the compounds as described herein withthe any adjuvants, excipients, or other desirable components asdescribed herein or known in the art and formulating, mixing, orcombining one or more additional active ingredients. The additionalactive ingredient may be, for example, an additional pesticide. Thepesticide may be, for example, an insecticide, a fungicide, anherbicide, or an additional nematicide as described herein or otherwiseknown in the art.

For example, a compound as described herein may be applied to seeds ortubers by impregnating them with a liquid seed treatment compositioncomprising a compound described herein, or by coating them with a solidor liquid composition comprising a compound described herein.

Seed treatment methods described herein can be used in connection withany species of plant and/or the seeds thereof as described herein. Insome embodiments, however, the methods are used in connection with seedsof plant species that are agronomically important. In particular, theseeds can be of corn, peanut, canola/rapeseed, soybean, cucurbits,crucifers, cotton, beets, rice, sorghum, sugar beet, wheat, barley, rye,sunflower, tomato, sugarcane, tobacco, oats, as well as other vegetableand leaf crops. In some embodiments, the seed is corn, soybean, orcotton seed. The seed may be a transgenic seed from which a transgenicplant can grow and incorporate a transgenic event that confers, forexample, tolerance to a particular herbicide or combination ofherbicides, insect resistance, increased disease resistance, enhancedtolerance to stress and/or enhanced yield. Transgenic seeds include, butare not limited to, seeds of corn, soybean and cotton.

A seed treatment method may comprise applying the seed treatmentcomposition to the seed prior to sowing the seed, so that the sowingoperation is simplified. In this manner, seeds can be treated, forexample, at a central location and then dispersed for planting. Thispermits the person who plants the seeds to avoid the complexity andeffort associated with handling and applying the compositions, and tomerely handle and plant the treated seeds in a manner that isconventional for regular untreated seeds.

A composition can be applied to seeds by any standard seed treatmentmethodology, including but not limited to mixing in a container (e.g., abottle or bag), mechanical application, tumbling, spraying, immersion,and solid matrix priming. Seed coating methods and apparatus for theirapplication are disclosed in, for example, U.S. Pat. Nos. 5,918,413;5,891,246; 5,554,445; 5,389,399; 5,107,787; 5,080,925; 4,759,945 and4,465,017, among others. Any conventional active or inert material canbe used for contacting seeds with the composition, such as conventionalfilm-coating materials including but not limited to water-based filmcoating materials.

For example, in one embodiment, a composition can be introduced onto orinto a seed by use of solid matrix priming. For example, a quantity ofthe composition can be mixed with a solid matrix material and then theseed can be placed into contact with the solid matrix material for aperiod to allow the composition to be introduced to the seed. The seedcan then optionally be separated from the solid matrix material andstored or used, or the mixture of solid matrix material plus seed can bestored or planted directly. Non-limiting examples of solid matrixmaterials which are useful include polyacrylamide, starch, clay, silica,alumina, soil, sand, polyurea, polyacrylate, or any other materialcapable of absorbing or adsorbing the composition for a time andreleasing the active compound of the composition into or onto the seed.It is useful to make sure that the active compound and the solid matrixmaterial are compatible with each other. For example, the solid matrixmaterial should be chosen so that it can release the active compound ata reasonable rate, for example over a period of minutes, hours, days, orweeks.

Imbibition is another method of treating seed with the composition. Forexample, a plant seed can be directly immersed for a period of time inthe composition. During the period that the seed is immersed, the seedtakes up, or imbibes, a portion of the composition. Optionally, themixture of plant seed and the composition can be agitated, for exampleby shaking, rolling, tumbling, or other means. After imbibition, theseed can be separated from the composition and optionally dried, forexample by patting or air drying.

A composition may be applied to the seeds using conventional coatingtechniques and machines, such as fluidized bed techniques, the rollermill method, rotostatic seed treaters, and drum coaters. Other methods,such as spouted beds may also be useful. The seeds may be pre-sizedbefore coating. After coating, the seeds may be dried and thentransferred to a sizing machine for sizing. Such procedures aregenerally known in the art.

If a composition is applied to the seed in the form of a coating, theseeds can be coated using a variety of methods known in the art. Forexample, the coating process can comprise spraying the composition ontothe seed while agitating the seed in an appropriate piece of equipmentsuch as a tumbler or a pan granulator.

In one embodiment, when coating seed on a large scale (for example acommercial scale), the seed coating may be applied using a continuousprocess. For example, seed may be introduced into the treatmentequipment (such as a tumbler, a mixer, or a pan granulator) either byweight or by flow rate. The amount of treatment composition that isintroduced into the treatment equipment can vary depending on the seedweight to be coated, surface area of the seed, the concentration of thefungicide and/or other active ingredients in a composition, the desiredconcentration on the finished seed, and the like. A composition can beapplied to the seed by a variety of means, for example by a spray nozzleor revolving disc. The amount of liquid may be determined by the assayof the formulation and the required rate of active ingredient necessaryfor efficacy. As the seed falls into the treatment equipment the seedcan be treated (for example by misting or spraying with the composition)and passed through the treater under continual movement/tumbling whereit can be coated evenly and dried before storage or use.

In another embodiment, the seed coating may be applied using a batchprocess. For example, a known weight of seeds can be introduced into thetreatment equipment (such as a tumbler, a mixer, or a pan granulator). Aknown volume of the composition can be introduced into the treatmentequipment at a rate that allows the composition to be applied evenlyover the seeds. During the application, the seed can be mixed, forexample by spinning or tumbling. The seed can optionally be dried orpartially dried during the tumbling operation. After complete coating,the treated sample can be removed to an area for further drying oradditional processing, use, or storage.

In an alternative embodiment, the seed coating may be applied using asemi-batch process that incorporates features from each of the batchprocess and continuous process embodiments set forth above.

In still another embodiment, seeds can be coated in laboratory sizecommercial treatment equipment such as a tumbler, a mixer, or a pangranulator by introducing a known weight of seeds in the treater, addingthe desired amount of the composition, tumbling or spinning the seed andplacing it on a tray to thoroughly dry.

In another embodiment, seeds can also be coated by placing the knownamount of seed into a narrow neck bottle or receptacle with a lid. Whiletumbling, the desired amount of the composition can be added to thereceptacle. The seed is tumbled until it is coated with the composition.After coating, the seed can optionally be dried, for example on a tray.

In some embodiments, the treated seeds may also be enveloped with a filmovercoating to protect the fungicidal coating. Such overcoatings areknown in the art and may be applied using conventional fluidized bed anddrum film coating techniques. The overcoatings may be applied to seedsthat have been treated with any of the seed treatment techniquesdescribed above, including but not limited to solid matrix priming,imbibition, coating, and spraying, or by any other seed treatmenttechnique known in the art.

Treated Seeds

In one embodiment the disclosure is generally related to a seed that hasbeen treated with a composition as described herein comprising acompound (e.g., a compound of Formula I, Ia, Ib, II, IIa, or IIb) asdescribed herein. In some embodiments, the seed has been treated withthe composition using one of the seed treatment methods set forth above,including but not limited to solid matrix priming, imbibition, coating,and spraying. The treated seed may be of any plant species, as describedabove. In other embodiments, a seed is treated with a composition asdescribed herein, including formulating, mixing in a seed treater tank,or combining on a seed by overcoating one or more additional activeingredients. The additional active ingredient may be, for example, anadditional pesticide. The pesticide may be, for example, an insecticide,a fungicide, an herbicide, or an additional nematicide as describedherein.

The amount of a compound present on a treated seed sufficient to protectthe seed, and/or the roots of a plant grown from the seed, againstdamage by phytopathogenic fungi can be readily determined by one ofordinary skill in the art. In an embodiment, treated seeds comprise acompound of Formula I, Ia, Ib, II, IIa, or IIb in an amount of at leastabout 0.005 mg/seed. In another embodiment, treated seeds comprise acompound of Formula I, Ia, Ib, II, IIa, or IIb in an amount of fromabout 0.005 to about 2 mg/seed, or from about 0.005 to about 1 mg/seed.

Administration

In some embodiments, a compound (e.g., a compound of Formula I, Ia, Ib,II, IIa, or IIb) as described herein is used as a ACCase modulator. Forexample, in some embodiments, the present disclosure is directed to amethod of modulating acetyl-CoA carboxylase (ACCase) in a biologicalorganisim, wherein the method comprises administering to the biologicalorganism a composition comprising an effective amount of a compound.

In some embodiments, the biological organism is an animal. For example,in some embodiments, the biological organism is a warm-blooded animal.In some embodiments, the biological organism is a mammal, including, forexample, humans.

A compound described herein may generally be formulated in a compositioncomprising one or more biologically acceptable excipients and,optionally, another pharmaceutically active agent known to those skilledin the art.

Any suitable dosage may be administered. The compound or salt thereofchosen for a particular application, the carrier and the amount willvary widely depending on the species of the warm blooded animal or humanor the particular disease condition being treated, and depending uponthe effective modulatory concentrations observed in trial studies. Thedosage administered will, of course, vary depending upon known factors,such as the pharmacodynamic characteristics of the particular compoundor salt thereof and its mode and route of administration; the age,health, or weight of the subject; the nature and extent of symptoms; themetabolic characteristics of the composition and patient, the kind ofconcurrent treatment; the frequency of treatment; or the effect desired.

A dosage unit may comprise a single compound, or mixtures thereof, withother compounds. The dosage unit may comprise diluents, extenders,carriers, liposomes, or the like. The unit may be in solid or gel formsuch as pills, tablets, capsules and the like or in liquid form suitablefor oral, rectal, topical, intravenous injection or parenteraladministration or injection into or around the treatment site.

Having described the disclosure in detail, it will be apparent thatmodifications and variations are possible without departing from thescope of the claims.

EXAMPLES

The following non-limiting examples are provided for furtherillustration.

Example 1 ACCase Enzymatic Assay

Ustilago maydis acetyl CoA carboxylase (ACCase) was cloned, expressed,and purified as described (Weatherly et al, Biochem. J., 2004) and thetest compounds were tested in a 96-well plate format. Primary in vitroscreening consisted of obtaining dose response data at 100, 33, 10, and1 μM inhibitor. Actives in the primary screen were re-tested toestablish IC50 values.

Direct detection of the conversion of acetyl CoA to malonyl CoA byACCase was not feasible, but during this process ATP is converted to ADPwhich allowed for detection through a standard reaction coupling withADP recycling to the oxidation of NADH. Thus, ACCase activity wasmeasured via kinetic OD340 measurements of the conversion of NADH to NADin a coupled reaction involving the conversion of phosphoenolpyruvate(PEP) to lactate.

The complete 200 ul reaction mixture contained 52.5 mM HEPES (pH8),2.625 mM MgCl₂, 1 mM ATP, 0.525 mM DTT, 11 mM NaHCO₃, 1% DMSO with orwithout inhibitor, 1× pyruvate kinase/lactate dehydrogenase (PK/LDH),0.3 mM NADH, 0.5 mM PEP, and 5 μg ACCase. The reactions were incubatedat 30° C. for 10 minutes and then initiated by the addition of 0.33 mMacetyl CoA. The initiated reactions were read immediately via platereader at OD340 and kinetic readings were acquired every 20 s for 15minutes while keeping the temperature at 30° C.

A slope of the kinetic curve was determined by using the 2 to 7 minutedata which was then calculated as percent inhibition relative to the noinhibitor control.

The primary screens were conducted in duplicate and the IC50's conductedin triplicate. Averages were reported along with standard deviationcalculation to generate error bars.

Each plate contained its own controls and consisted of a DMSO onlycontrol, 5-fold titration series of soraphen from 2 μM to 3.2 nM, and anADP coupled reaction control.

In order to effectively screen out non-specific modulators of pyruvatekinase and lactate dehydrogenase (the coupled portion of the reaction),a PK/LDH inhibition test was developed. The complete 200 μl reactionmixture contained 52.5 mM HEPES (pH8), 2.625 mM MgCl₂, 0.525 mM DTT, 11mM NaHCO₃, 1% DMSO with or without inhibitor, 1× pyruvate kinase/lactatedehydrogenase (PK/LDH), 0.3 mM NADH, and 0.5 mM PEP. The reactions wereincubated at 30° C. for 10 minutes and then initiated by the addition of66 μM ADP. The initiated reactions were read immediately via platereader at OD340 and kinetic readings were acquired every 20 s for 15minutes while remaining at 30° C.

A slope of the kinetic curve was determined by using the 2 to 7 minutedata which was then calculated as percent inhibition relative to the noinhibitor control. Those compounds which had no significant PK/LDHinhibition at or above the IC50 in the ACCase assay, were considered tobe valid modulators of only ACCase. The IC50 data for compounds ofFormulas I and II are shown in Table 1A below.

TABLE 1 ACCase Inhibitory Activity IC50 Formula Name Structure (μM) Ia-i2-((4-(4-chlorophenyl)-3- cyano-6-(thiophen-2-yl)pyridine-2-yl)thio)-2-phenylacetic acid

   0.370^(a) Ia-ii 2-((3-cyano-6-(thiophen-2-yl)-4-(trifluoromethyl)pyridin- 2-yl)thio)-2-phenylacetic acid

   2.015^(a) Ia-iii 2-((3-cyano-4,6-di(thiophen-2-yl)pyridin-2-yl)thio)-2- phenylacetic acid

   0.616^(a) Ia-iv 2-((3-cyano-4-phenyl-6- (thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetic acid

   0.492^(a) Ia-v 2-((3-cyano-4-(4- methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2- phenylacetic acid

   0.119 Ia-vi 2-((3-cyano-8-methyl-4- (thiophen-2-yl)-5,6,7,8-tetrahydro-1,8-naphthyridin- 2-yl)thio)-2-phenylacetic acid

   3.549 Ia-vii 2-((4-cyano-1-(thiophen-2-yl)-5,6,7,8-tetrahydroisoquinolin- 3-yl)thio)-2-phenylacetic acid

   3.805 Ia-viii 2-((3-cyano-6-(2,4- dimethoxyphenyl)-4-(trifluoromethyl)pyridin-2- yl)thio)-2-phenylacetic acid

   1.718 Ia-ix 2-((3-cyano-6-(3,4- dimethoxyphenyl)-4-(trifluoromethyl)pyridin-2- yl)thio)-2-phenylacetic acid

   1.600 Ia-x 2-((6-(4-bromophenyl)-3-cyano- 4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylacetic acid

   1.946 Ia-xi 2-((3-cyano-6-(furan-2-yl)-4- (trifluoromethyl)pyridin-2-yl)thio-2-phenylacetic acid

   5.432 Ia-xii 2-((3-cyano-4,6-diphenylpyridin-2-yl)thio)-2-phenylacetic acid

   0.266 Ia-xiii 2-((3-cyano-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinolin- 2-yl)thio)-2-phenylacetic acid

   0.274 Ia-xiv 2-((3-cyano-4-(4- methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2- phenylacetic acid

   0.060 Ia-xv 2-((4-cyano-1-ethyl-5,6,7,8- tetrahydroisoquinolin-3-yl)thio)-2-phenylacetic acid

  10.24 Ia-xvi 2-((3-cyano-6-methyl-4- (trifluoromethyl)pyridin-2-yl)thio)-2-phenylacetic acid

   7.729 Ia-xvii 2-((3-cyano-4-phenyl-5,6,7,8-tetrahydroquinolin-2-yl)thio)- 2-phenylacetic acid

   0.906 Ia-xviii 2-((4-(4-chlorophenyl)-3-cyano-5,6,7,8-tetrahydronaphthalen-2- yl)thio)-2-phenylacetic acid

   1.385 Ia-xix 2-((4-(4-methoxyphenyl)-6- (thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetic acid

   9.059 Ia-xx 2-((3-cyano-6-(furan-2-yl)-4- (4-methoxyphenyl)pyridin-2-yl)thio)-2-phenylacetic acid

   0.345 Ia-xxi 2-((3-cyano-6-(thiophen-2-yl)-4-(p-tolyl)pyridin-2-yl)thio)- 2-phenylacetic acid

   0.353 Ia-xxii 2-((3-cyano-4-(4-fluorophenyl)-6-(thiophen-2-yl)pyridin-2- yl)thio)-2-phenylacetic acid

   0.563 Ia-xxiii 2-((4-(4-bromophenyl)-3-cyano-6-(thiophen-2-yl)pyridin- 2-yl)thio)-2-phenylacetic acid

   0.212 Ia-xxiv 2-((3-cyano-6-(furan-2-yl)-4- (thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetic acid

   0.958 Ia-xxv 2-((3-cyano-4,6-di(furan-2- yl)pyridin-2-yl)thio)-2-phenylacetic acid

   4.035 Ia-xxvi 2-((3-cyano-4-(4- methoxyphenyl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)- 2-phenylacetic acid

   0.56 Ia-xxvii 2-((3-cyano-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinolin- 2-yl)oxy)-2-phenylacetic acid

   0.249 Ia-xxviii 2-((3-cyano-4-(4- methoxyphenyl)-6-(1-oxidothiophen-2-yl)pyridin-2- yl)oxy)-2-phenylacetic acid

   0.196 Ia-xxix 2-((3-cyano-4-(4- methoxyphenyl)-6-(thiophen-2-yl)pyridin-2- yl)thio)butanoic acid

   0.113 Ib-i 2-((3-cyano-4-(thiophen-2- yl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylacetamide

   0.712 Ib-ii 2-((3-cyano-4-(4- methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2- phenylacetamide

>33 Ib-iii 2-((3-cyano-4-(4- methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-N- hydroxy-2-phenylacetamide

   0.882 IIb-i 2-((2-hydroxy-1- phenylethyl)thio)-4-(4-methoxyphenyl)-6-(thiophen- 2-yl)nicotinonitrile

   0.625 IIb-ii 2-((2-hydroxy-1- phenylethyl)thio)-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinoline- 3-carbonitrile

   4.093 IIb-iv 4-(furan-2-yl)-2-((2-hydroxy- 1-phenylethyl)thio)-6-(thiophen-2-yl)nicotinonitrile

   2.184 Soraphen    0.0458^(a) ^(a)IC50 values are a result of two ormore experiments

TABLE 1B ACCase Inhibitory Activity of Racemic Mixtures and SingleEnantiomers Formula Name Retention Time IC50 (μM) Ia-ii racemate 2.02Ia-ii-e1 enantiomer 1*  9.75 min 12.86 Ia-ii-e2 enantiomer 2  7.89 min1.208 Ia-iii racemate 0.439 Ia-iii-e1 enantiomer 1* 14.87 min 0.547Ia-iii-e2 enantiomer 2 18.51 min 2.39 Ia-xiv racemate 0.092; 0.14 Ia-xiv-e1 enantiomer 1* 15.64 min 0.115; 0.129 Ia-xiv-e2 enantiomer 218.13 min  0.44; 0.523 *More active enantiomer with a shorter retentiontime on the analytical Chiralpak IC column

Example 2 Fungal Growth Inhibition Assay

Spores were isolated from previously sub-cultured plates of Botrytiscinerea, Phytophthora capsici, Fusarium moniliforme, Fusariumviguliforme, Collectotrichum graminicola, and Diplodia maydis. Allspores were filtered and collected in a sterile glass bowl to isolatethe spores from the mycelia. The isolation and sub-culture platecondition for each pathogen is described below.

Spore isolation for B. cinerea: A 2-3 week old V8 (17%)+CaCO₃ (3 g/L)+20g agar plate was removed from room temperature and the mycelia weretreated with 5-10 ml of filter sterilized Triton X 100 (0.05%). Themycelia were scraped to re-suspend the spores. The spores were thencollected in a sterile filter bowl containing a fluted piece of filterpaper and poured into a conical tube.

Spore isolation for F. moniliforme: A 1 week old PDA (potato dextroseagar, pre-mix) plate was removed from 26° C. incubator with a light/dark12 hour cycle and the mycelia were treated with 5-10 ml of filtersterilized Triton X 100 (0.05%). The mycelia were scraped to re-suspendthe spores. The spores were then collected in a sterile filter bowlcontaining a fluted piece of filter paper.

Spore isolation for C. graminicola: A 1-2 week old oatmeal agar(pre-mix) plate was removed from 26° C. incubator with a light/dark 12hour cycle and the mycelia were treated with 10-15 ml of filtersterilized distilled water. The mycelia were scraped to re-suspend thespores. The spores were then collected in a sterile filter bowlcontaining a piece of sterile cheesecloth and poured into a conicaltube.

Spore isolation for F. virguliforme: A 2-3 week old PDA (pre-mix) platecontaining cefotaxime (100 mg/L) and kanamycin (50 mg/L) was removedfrom 26° C. incubator with a light/dark 12 hour cycle and the myceliawere treated with 5-10 ml of filter sterilized distilled water. Themycelia were scraped to re-suspend the spores. The spores were thencollected in a sterile filter bowl containing a fluted piece of filterpaper and poured into a conical tube.

Spore isolation for D. maydis: A 3-4 week old PDA (pre-mix) plate wasremoved from 26° C. incubator with a light/dark 12 hour cycle and themycelia were treated with 6-7 ml of sterile distilled water, scrapedinto a sterile petri dish, and smashed to open the pycnidia. The sporeswere then collected in a sterile filter bowl containing a fluted pieceof filter paper and poured into a conical tube.

Spore isolation for P. capsici: Three to five days prior to the assay a2-3 week old V8 (17%)+CaCO₃ (3 g/L)+20 g agar plate was removed from adark 25° C. incubator and cut up into small chunks. One plate wasseparated into two deep well plates and rinsed with sterile distilledwater three times. The cut up pieces were incubated under light in asterile filter hood with 25 ml of sterile distilled water. On the day ofthe assay the water was removed and 5-7 ml of fresh sterile distilledwater was added. One plate was incubated at 4° C. for 45-60 minutes andthen placed at room temperature for about 45-60 minutes. The spores werecollected in a sterile filter bowl containing a fluted piece of filterpaper. The spores were vortexed in a conical tube for 30-60 seconds toremove the flagella of the zoospores after isolation.

After spore isolation, pathogen spores were counted on a hemocytometerto calculate the spores/ml. In 17% V8 liquid media containing 3 g/LCaCO₃, isolated spores were diluted to individual concentrations basedon the growth curves at 48 hours of each pathogen. The sporeconcentrations for each pathogen were as follows: B. cinerea—10,000sp/ml; P. capsici—300 sp/ml; F. monliforme—500 sp/ml; F.virguliforme—500 sp/ml; C. graminicola—3,000 sp/ml; and D. maydis—3,000sp/ml.

Chemistry stocks were dissolved in DMSO at 2.5 mg/ml. Chemistry wasdiluted in a 96-well stock plate in five-fold dilutions to obtain afinal concentration of 50, 10, and 2 ppm in vitro. The finalconcentration of the positive control after the five-fold dilutions wasas follows: soraphen—0.5, 0.1, and 0.02 ppm. Negative controls on eachplate included 2% DMSO, water containing spores and media, and a blankfor background subtraction.

In a 96-well plate the spore solution, chemistries, and controls werecombined to make the final solution concentrations mentioned above. Uponaddition of the chemistry, an OD600 reading was done to assess chemicalprecipitation. The 96-well plates were incubated in plastic tubscontaining wet paper towels under the following conditions, 25° C. inthe dark for P. capsici and B. cinerea or 26° C. with light/dark cyclefor C. graminicola, D. maydis, F. virguliforme, F. monliforme. Platereadings were repeated at 24 and 48 hrs. Visual ratings were performedat 24 and 48 hrs to check for precipitation and confirm efficacy. Visualand OD600 ratings of the chemistry at 48 hours were compared to the 2%DMSO control to determine the percent of pathogen growth inhibition.

Fungal growth inhibition data for compounds of Formula I against severalfungal species are shown in Table 2A through 2E.

TABLE 2A Fungal Growth Inhibition of Collectotrichum graminicola C.graminicola % growth inhibition at 48 hours Formula 50 ppm 10 ppm 2 ppmIa-i 92 72 28 Ia-iii 91 98 27 Ia-iv 76 41 5 Ia-v 79 32 0 Ia-vii 71 19 11Ia-ix 72 17 5 Ia-xii 80 35 6 Ia-xiv 79 32 6

TABLE 2B Fungal Growth Inhibition of Diplodia maydis D. maydis % growthinhibition at 48 hours Formula 50 ppm 10 ppm 2 ppm Ia-i 65 57 3 Ia-iii82 87 0 Ia-v 52 61 0 Ia-vii 64 46 11 Ia-ix 70 37 32 Ia-xi 82 54 38Ia-xii 86 59 42 Ia-xiii 40 13 20

TABLE 2C Fungal Growth Inhibition of Fusarium virguliforme F.virguliforme % growth inhibition at 48 hours Formula 50 ppm 10 ppm 2 ppmIa-iii 90 84 2 Ia-xv 48 10

TABLE 2D Fungal Growth Inhibition of Botrytis cinerea B. cinerea %growth inhibition at 48 hours Formula 50 ppm 10 ppm 2 ppm Ia-x 25 12 0Ia-xii 19 6 0 Ia-xiv 8 14 Ia-xxviii 27 14

TABLE 2E Fungal Growth Inhibition of Phytophthora capsici P. capsici %growth inhibition at 48 hours Formula 50 ppm 10 ppm 2 ppm Ia-iv 90 11 0Ia-vii 100 9 0 Ia-ix 34 39 10 Ia-xii 22 36 16

Example 3 Yeast Growth Inhibition Assay

Yeast cells (Ade2 strain) were grown in liquid YPD (1% yeast extract, 2%peptone, 2% dextrose) for 16 hours at 30° C. from previouslysub-cultured plates of Saccharomyces cerevisiae. The OD600 of theovernight culture was checked via spectrophotometer and diluted to aconcentration of 2×10⁴ cells/ml.

Chemistry stocks were dissolved in DMSO to a concentration of 10 mM.Chemistry stocks were further diluted in a 96-well stock plate to obtainfinal concentrations of 100, 33, 10 and 1 μM in 1% DMSO. The finalconcentrations of the soraphen positive controls were 400, 40, and 3.2nM. The negative controls on each plate included a backgroundsubtraction control containing yeast and 1% DMSO (without chemistry) anda second contamination control containing YPD (with no yeast) and 1%DMSO (without chemistry).

98 μl liquid YPD was added to 2 μl diluted stock of DMSO per well andmixed thoroughly. After mixing, 100 μl of the diluted yeast solution wasadded to bring the final yeast concentration to 1×10⁴ cells/ml or 2000cells per well. An initial spectrophotometric reading at OD600 wasconducted on the entire plate and served as the 0 hour time point usedto subtract any background. The plate was then incubated for 24 hours at30° C. with mild shaking. At the 24 hour time point all wells of theplate were re-suspended by pipette to yield a uniform suspension, thenread again at OD600. The OD600 reading at 0 hours (background) wassubtracted from the 24 hour OD600 reading and all wells were compared tothe negative control and subtracted from 100 to determine the percentinhibition. All experiments were conducted in triplicate. Averages werereported along with standard deviation calculation to generate errorbars. Each plate contained its own controls and consisted ofinoculated+DMSO, non-inoculated+DMSO, and a titration series of soraphenat 400, 40, and 3.2 nM. The results of growth inhibition forSaccharomyces cerevisiae are reported in Table 3 below.

TABLE 3 Growth Inhibition of Saccharomyces cerevisiae S. cerevisiae %growth inhibition at 48 hours Formula 100 μM 33.3 μM 11.1 μM 3.7 μMIa-viii 100 62 23 6 Ia-x 99 46 13 12 Ia-ii 51 12 0 7

Description of Synthesis of Compounds Described Herein

Generally, the compounds of Formulas I, Ia, Ib, II, IIa, and IIb may beprepared using methods known to those skilled in the art.

Example 4 Description of Synthesis of Compounds of Formula I

For example, compounds of Formula I can be prepared as set forth inScheme 1 below. More particularly, the synthesis of compound 5 startswith the preparation of pyridine derivative 3 from a diketone 1 andcyanoacetamide 2, followed by alkylation with 1-bromophenyl acetic acid4 in presence of aqueous KOH in acetone. Alternatively, alkylation canbe accomplished with methyl α-bromophenylacetate and K₂CO₃ via formationof a methyl ester derivative 7 and subsequent hydrolysis with 1N NaOH toafford a desired carboxylic acid compound 5. The racemate compound 5 canbe separated into single enantiomers by preparative HPLC using a chiralstationary column.

Substituents E and R⁶ may be selected as set forth with regard toFormula I above.

Alternatively, the compounds of Formula I may be prepared as generallyset forth in Scheme 2 below. The general method depicted in Scheme 2involves the formation of pyridine derivatives 5 from chalcone 3 and a2-cyanoacetamide 4 in ethanol (EtOH) in the presence of catalytic amountof pyridine. The chalcone 3 can be prepared, for example, by aClaisen-condensation of the corresponding aldehyde 2 and acetyl-compound1 in presence of aqueous NaOH in ethanol. Alkylation of pyridinederivative 5 with methyl α-bromophenylacetate 6 can be performed in thepresence of K₂CO₃ in acetone. The saponification of the methyl ester 7may be achieved with aqueous 1N LiOH in tetrahydrofuran (THF)/methanol(MeOH) mixture to yield the final product 8.

Substituents E and R⁴ through R⁶ may be selected as set forth withregard to Formula I above.

In a further alternative, the compounds of Formula I may be prepared asgenerally set forth in Scheme 3 below. Substituents E and R⁴ through R⁶may be selected as set forth with regard to Formula I above.

As used in Scheme 3 below, the abbreviation “NEt₃” refers totriethylamine.

In a further alternative, the compounds of Formula I may be prepared asgenerally set forth in Scheme 4 below. More particularly, the methoddisclosed in Scheme 4 involves the formation of the thiopyridinederivative 5 via the thiopyran-intermediate 4, which is subsequentlytreated with the cyclohexanone-morpholine enamine.

Substituents E, R⁴, and R⁶ may be selected as set forth with regard toFormula I above.

In a further alternative, compounds of Formula I may be prepared asgenerally set forth in Scheme 5 below. Scheme 5 is particularly suitablefor the preparation of compounds wherein R⁴ is heteroaryl.

More particularly, the process involves reaction of the2-cyanothioacetamide 2 and the heteroaryl carboxaldehyde 1, followed byreaction with cyclohexanone to give the desired thiopyridine derivative2. Alkylation of intermediate 2 with methyl α-bromophenylacetate,followed by saponification yields the product compound 5. Generally,substituent R⁴ may be selected as set forth with regard to Formula Iabove.

In a further alternative, compounds of Formula I may be prepared asgenerally set forth in Scheme 6 below. Scheme 6 is particularly suitablefor the preparation of compounds wherein R³ is hydrogen.

In a first step of the process, the chalcone 1 is treated with acetylglycinamide in the presence of cesium carbonate andN,N-dimethylformamide (DMF) to give 2-hydroxypyridine 3. Theintermediate 3 can be transformed with Lawesson's reagent to form thecorresponding thiopyridine derivatives 4, followed by alkylation to formthe methyl ester intermediate 6 and saponification to form the finalproduct 7.

Alternatively, the intermediate 3 can be alkylated with methylα-bromophenylacetate to form corresponding compounds of Formula Iwherein the E substituent is O. Substituents R⁴ and R⁶ may be selectedas generally set forth with regard to Formula I above.

Example 5 Description of Synthesis of Compounds of Formula I

Compounds of Formula I may be prepared as set forth in exemplary Scheme7 below. Substituents E and R³ through R⁶ may be selected as generallyset forth with regard to Formula I above.

As used in Scheme 7 below, “AIBN” refers to azobisisobutyronitrile.

Alternatively, compounds of Formula I may be prepared as set forth inexemplary Scheme 8 below. Generally, preparation of the the pyridinederivative 5 may be accomplished using the same procedure as depicted inScheme 7 above. The corresponding alcohol 7 is then prepared byalkylation of the pyridine derivative 5 with 2-bromo-2-phenylethanol 6.Substituents E and R³ through R⁶ may be selected as generally set forthwith regard to Formula I above.

Example 6 Description of Synthesis of Compounds of Formula II

Compounds of Formula IIa may be prepared as set forth in exemplaryScheme 9 below. More particularly, preparation of the the pyridinederivative 5 may be accomplished using the same procedure as depicted inScheme 7 above. Compound 5 can then be alkylated with5-benzyl-2-trityl-tetrazole 4 to give, following deprotection, thecorresponding tetrazole product 7. Substituents E and R⁴ through R⁶ maybe selected as generally set forth with regard to Formula IIa above.

As used in Scheme 9 below, the abbreviation “TMSN₃” refers totrimethylsilyl azide, the abbreviation “TBAF” refers totetra-n-butylammonium fluoride, and the abbreviation “DCM” refers todichloromethane.

Example 7 General Procedure for the Preparation of Compounds of FormulaI According to Exemplary Scheme 2

The following compounds and procedures, each of which is referenced inexemplary Scheme 2 above, were prepared and/or carried out using as setforth in detail below.

General Procedure of Preparation of Chalcones 3

Sodium hydroxide (3N, 46 mL, 3 equiv.) was added to a mixture of ketone1 (46 mmol, 1 equiv.) and aldehyde 2 (46 mmol, 1 equiv.) in ethanol (100mL). The mixture was stirred for 4 h. The resulting precipitate wasfiltered off and washed with a litte ethanol and water. The solid wasdried in the air to afford the desired chalcone 3. If there was noprecipitate water was added. The mixture was extracted with ethylacetate (3×). The combined organic layers were dried over Na₂SO₄ andconcentrated in vacuo. The residue was purified with automated columnchromatography (SiO₂, heptane/ethyl acetate, gradient).

General Procedure of Preparation of Thiopyridine Derivatives 5

A mixture of chalcone 3 (5 mmol, 1 equiv.), 2-cyanothioacetamide (5mmol, 1 equiv.) and a catalytic amount of piperidine (0.1 mL) in ethanol(20 mL) was refluxed for 5 hours. The mixture was cooled down to roomtemperature. The resulting precipitate was filtered off and dried in theair affording the pyridine derivatives 5 in yields varying from 10 to30%. If there was no precipitate water was added (10 mL) to induceprecipitation. The resulting precipitate was filtered off and dried inair.

If there was still no precipitate, the mixture was allowed to standovernight and was then decanted. The residue was purified with columnchromatography (SiO₂, heptane/ethyl acetate, gradient).

General Procedure of Alkylation of Pyridine Derivative 5

A mixture of pyridine derivatives 5 (1.0 equiv.), K₂CO₃ (1.1 equiv.) andmethyl 1-bromo-phenylacetate (1.1 equiv.) in acetone (15 mL) wasrefluxed for 2 hours. The mixture was cooled to room temperature andfiltered. The filtrate was concentrated to yield the desired methylester derivatives 7. If necessary purification was performed with anautomated column chromatography (SiO₂, heptane/ethyl acetate, gradient).

General Procedure of Saponification of the Methylester Derivatives 7.

NaOH (1N, 2 mL) was added to a mixture of 7 (1 mmol) in THF (2 mL) andmethanol (2 mL). After 4 h the mixture was concentrated and stripped todryness with toluene. The residue was suspended in ethyl acetate andfiltered. The filtrate was washed with ethyl acetate, until the filtratewas colorless. The solid was dissolved in water and the solution wasacidified with 1N HCl. The resulting precipitate was filtered off andwashed with a little water. The solid was dried to the air to afford anoff-white solid.

Unless otherwise noted, the general procedures described above were usedto synthesise these compounds, to the extent that they appear, in thefurther examples below.

Example 8 Preparation of2-((3-cyano-6-(thiophen-2-yl)-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylaceticAcid (Formula Ia-ii)

2-Cyanoethanethioamide (1.4 g, 13.5 mmol) was added to a solution of4,4,4-trifluoro-1-(thiophen-2-yl)butane-1,3-dione (3.0 g, 13.5 mmol) andtriethylamine (3.0 mL) in ethanol (10 mL). The resulting mixture wasrefluxed for 2 hours, and then diluted with water (20 mL). Theprecipitate was filtered and washed with water (3×20 mL) and dried inair to give triethylamine salt of2-mercapto-6-(thiophen-2-yl)-4-(trifluoromethyl)nicotinonitrile (4.25 g,11.0 mmol, 81%) as a yellow solid.

Aqueous KOH (10%, 0.56 mL) was added to a solution of the triethylaminesalt of 2-mercapto-6-(thiophen-2-yl)-4-(trifluoromethyl)-nicotinonitrile(387 mg, 1.0 mmol) in ethanol, followed by the addition ofalpha-bromophenyl acetic acid (215 mg, 1.0 mmol). The mixture wasrefluxed for 3 hours and cooled to room temperature. The organic solventwas removed in vacuo and H₂O (20 mL) was added to the residue. The pHwas adjusted to 6 with 1M HCl. The precipitate was filtered off andwashed with H₂O (3×20 mL) and dried in air to give racemic2-((3-cyano-6-(thiophen-2-yl)-4-(trifluoromethyl)-pyridin-2-yl)thio)-2-phenylaceticacid (370 mg, 0.88 mmol, yield 88%) as a reddish solid. LC-MS [M+H] 421(C₁₉H₁₁F₃N₂O₂S₂+H, requires 421.02).

A portion of the racemic product (200 mg) was separated into enantiomersby preparative HPLC on a chiral stationary column (Chiralpak IA-column,20×250 mm, Flow 10 ml/min) using as a mobile phase a mixture ofheptane/ethanol/trifluoroacetic acid (85/15/0.2) to yield 63 mg ofenantiomer 1 (Formula Ia-ii-e1) and 66 mg of enantiomer 2 (FormulaIa-ii-e2). Both enantiomers were analyzed for enantiomeric purity byHPLC using Chiralpak IC-column (0.46×20) and as a mobile phase a mixtureof heptane/ethanol/trifluoroacetic acid (75/20/0.2) at 0.7 ml/min flowrate. The enantiomeric excess (ee) of the Enantiomer 1 (FormulaIa-ii-e1) that was eluted at R_(t)=9.75 min was determined to be 97.3%and Enantiomer 2 (Formula Ia-ii-e2) that was eluted at Rt=7.89 min was99.8%, respectively. LC-MS and ¹H-NMR spectra for both enantiomers werein accordance with the chemical structure. LC-MS LC-MS [M+H] 421(C₁₉H₁₁F₃N₂O₂S₂+H, requires 421.02).

The absolute configuration of the enantiomer 2 (Formula Ia-ii-e2) wasresolved by X-ray crystallography analysis and found to be the Sconfiguration (see FIG. 1).

Table 4 below contains the x-ray crystallographic coordinates forenantiomer 2. The coordinates are listed in Angstroms. Enantiomer 2crystallized in a unit cell with dimensions of a=5.257 Å, b=8.096 Å,c=19.325 Å with alpha=beta=gamma angles equal to 90° in a P 21 21 21space group.

TABLE 4 X-ray crystallographic coordinates, space group and unit cellfor Enantiomer 2 (Formula Ia-ii-e2) Atom Atom temparature Number Type xy z occupancy factor ATOM 1 1 S1 4.517 16.195 3.23 1 1.11 ATOM 2 2 F16.562 13.107 7.178 1 2.46 ATOM 3 3 F2 5.123 11.551 7.448 1 2.67 ATOM 4 4F3 4.745 13.498 8.234 1 2.48 ATOM 5 5 O1 4.048 14.287 0.878 1 1.25 ATOM6 6 O2 1.873 14.852 0.719 1 1.25 ATOM 7 7 H2 1.825 14.161 0.243 1 1.87ATOM 8 8 N1 3.086 13.988 3.683 1 1.01 ATOM 9 9 N2 6.751 16.049 5.911 11.84 ATOM 10 10 C1 3.205 16.256 1.987 1 0.98 ATOM 11 11 H1 2.33 16.4262.44 1 1.17 ATOM 12 12 C2 3.507 17.402 1.034 1 0.93 ATOM 13 13 C3 2.63118.467 0.932 1 1.26 ATOM 14 14 H3 1.874 18.513 1.505 1 1.51 ATOM 15 15C4 2.852 19.465 0.001 1 1.58 ATOM 16 16 H4 2.25 20.197 −0.063 1 1.89ATOM 17 17 C5 3.953 19.395 −0.837 1 1.49 ATOM 18 18 H5 4.101 20.075−1.483 1 1.79 ATOM 19 19 C6 4.834 18.338 −0.735 1 1.44 ATOM 20 20 H65.591 18.295 −1.307 1 1.72 ATOM 21 21 C7 4.617 17.34 0.199 1 1.26 ATOM22 22 H7 5.225 16.614 0.27 1 1.51 ATOM 23 23 C8 3.101 14.994 1.161 10.97 ATOM 24 24 C9 4.086 14.746 4.125 1 0.99 ATOM 25 25 C10 4.853 14.4285.26 1 1.02 ATOM 26 26 C11 4.562 13.235 5.918 1 1.1 ATOM 27 27 C12 3.56512.425 5.438 1 1.19 ATOM 28 28 H12 3.371 11.6 5.866 1 1.43 ATOM 29 29C13 2.835 12.822 4.312 1 1.02 ATOM 30 30 C14 5.916 15.311 5.648 1 1.22ATOM 31 31 C15 5.256 12.849 7.194 1 1.42 ATOM 32 32 C16A 1.771 12.0143.744 0.799 0.97 ATOM 33 33 C17A 0.833 12.31 2.781 0.799 1.49 ATOM 34 34H17A 0.817 13.138 2.316 0.799 1.79 ATOM 35 35 C18A −0.088 11.3 2.5460.799 1.24 ATOM 36 36 H18A −0.797 11.371 1.917 0.799 1.48 ATOM 37 37C19A 0.132 10.199 3.311 0.799 1.36 ATOM 38 38 H19A −0.394 9.409 3.2740.799 1.63 ATOM 39 39 S2A 1.479 10.412 4.353 0.799 1.44 ATOM 40 40 C16B1.757 11.936 3.921 0.201 0.97 ATOM 41 41 C17B 1.439 10.678 4.309 0.2011.49 ATOM 42 42 H17B 1.864 10.208 5.017 0.201 1.79 ATOM 43 43 C19B 0.41710.175 3.54 0.201 1.36 ATOM 44 44 H19B 0.035 9.32 3.703 0.201 1.63 ATOM45 45 C18B −0.008 10.973 2.541 0.201 1.24 ATOM 46 46 H18B −0.694 10.751.923 0.201 1.48 ATOM 47 47 S2′B 0.868 12.452 2.544 0.201 1.44

Example 9 Preparation of methyl2-((3-cyano-6-(thiophen-2-yl)-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylacetate(Formula IIb-iii)

A mixture of triethylamine salt of2-mercapto-6-(thiophen-2-yl)-4-(trifluoromethyl)-nicotinonitrile (387mg, 1.0 mmol), methyl α-bromophenylacetate (225 mg, 1.0 mmol) and K₂CO₃(150 mg, 1.1 mmol) in acetone (10 mL) was refluxed for 2 hours under aN₂-atmosphere. The mixture was cooled to room temperature and filtered.The filtrate was concentrated in vacuo to give methyl2-((3-cyano-6-(thiophen-2-yl)-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylacetate(380 mg, 0.87 mmol, yield 87%) as a yellowish solid with an HPLC purityof 94.4%. LC-MS [M+H] 435 (C₂₀H₁₃F₃N₂O₂S₂+H, requires 435.04). The¹H-NMR spectrum was in accordance with the chemical structure.

Example 10 Preparation of2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticAcid (Formula Ia-xiv)

The reaction of 2-acetylthiophene (2.05 mL, 2.38 g, 18.9 mmol) andp-anisaldehyde (2.3 mL, 18.9 mmol) afforded chalcone(E)-3-(4-methoxyphenyl)-1-(thiophen-2-yl)prop-2-en-1-one with 89% yield(4.13 g, 16.9 mmol) as an off-white solid (Obtained by precipitation).The ¹H-NMR spectrum was in accordance with the chemical structure.

The reaction of chalcone(E)-3-(4-methoxyphenyl)-1-(thiophen-2-yl)prop-2-en-1-one (1.5 g, 6.1mmol) with 1 equivalent 2-cyanothioacetamide afforded the desiredthiopyridine derivative that was purified by silica gel chromatography.The pure4-(4-methoxyphenyl)-6-(thiophen-2-yl)-2-thioxo-1,2-dihydropyridine-3-carbonitrilewas obtained with 24% yield (470 mg, 1.4 mmol) as an orange solid. The¹H-NMR spectrum was in accordance with the chemical structure.

Alkylation of the4-(4-methoxyphenyl)-6-(thiophen-2-yl)-2-thioxo-1,2-dihydropyridine-3-carbonitrile(214 mg, 0.66 mmol) with methyl α-bromophenylacetate (167 mg, 0.73 mmol,1.1 equiv.) afforded after purification methyl2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetatewith 78% yield (242 mg, 0.51 mmol) as an off-white solid afterprecipitation from ethyl acetate (3 mL). The ¹H-NMR spectrum was inaccordance with the chemical structure.

The saponification of the methyl2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetate(242 mg, 0.530 mmol) was carried out with 1N NaOH in the THF/methanolmixture and the desired product2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid was isolated as described in the general procedure.

The racemic crude product was separated into enantiomers by preparativeHPLC on a chiral stationary column (Chiralpak IC-column, 20×250 mm, Flowrate at 17 ml/min) using as a mobile phase a mixture ofheptane/ethanol/trifluoroacetic acid (80/20/02) to yield 30 mg (0.065mmole, yield 12%) of enantiomer 1 (Formula Ia-xiv-e1) as off-white solidand 33 mg (0.074 mmol, yield 14%) of enantiomer 2 (Formula Ia-xiv-e2) asoff-white soild. Both enantiomers were analyzed for enantiomeric purityby HPLC using Chiralpak IC-column (0.46×25) and as a mobile phase amixture of heptane/ethanol/trifluoroacetic acid (80/20/02) at 0.7 ml/minflow rate. The enantiomeric excess (ee) of the Enantiomer 1 (FormulaIa-xiv-e1) that was eluted at R_(t)=15.64 min was determined to be 99.3%and Enantiomer 2 (Formula Ia-xiv-e2) that was eluted at R_(t)=18.13 minwas 99.2%, respectively. LC-MS and The ¹H-NMR spectra for bothenantiomers are in accordance with the chemical structure. LC-MS LC-MS[M+H] 459.1 (C₂₅H₁₈N₂O₃S₂+H, requires 459.08).

Example 11 Preparation of2-((3-cyano-4,6-di(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetic Acid(Formula Ia-iii)

The reaction of 2-acetylthiophene (2.5 mL, 23.0 mmol) and 2-thiophenecarboxaldehyde (2.15 mL, 23.0 mmol) afforded chalcone(E)-1,3-di(thiophen-2-yl)prop-2-en-1-one with 93% yield (4.7 g, 21.3mmol) as a brown solid (Obtained by precipitation). The ¹H-NMR spectrumwas in accordance with the chemical structure.

The reaction of chalcone(E)-3-(4-methoxyphenyl)-1-(thiophen-2-yl)prop-2-en-1-on (1.5 g, 6.1mmol) with 1 equivalent 2-cyanothioacetamide afforded the desiredthiopyridine derivative that was purified by silica gel chromatography.The pure4-(4-methoxyphenyl)-6-(thiophen-2-yl)-2-thioxo-1,2-dihydropyridine-3-carbonitrilewas obtained with a 24% yield (470 mg, 1.4 mmol) as an orange solid. The¹H-NMR spectrum was in accordance with the chemical structure.

Alkylation of the4-(4-methoxyphenyl)-6-(thiophen-2-yl)-2-thioxo-1,2-dihydropyridine-carbonitrile(500 mg, 1.7 mmol) with methyl α-bromophenylacetate (428 mg, 1.87 mmol,1.1 equiv.) afforded methyl2-((3-cyano-4,6-di(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetate (150mg, 0.33 mmol, 20%) as a beige solid. The ¹H-NMR spectrum was inaccordance with the chemical structure.

The saponification of the methyl2-((3-cyano-4,6-di(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetate (150mg, 0.330 mmol) was carried out with 1N NaOH in the THF/methanol mixtureand the crude product2-((3-cyano-4,6-di(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetic acidwas isolated using the general procedure as described in the examplesabove.

The racemic acid product was separated into enantiomers by preparativeHPLC on a chiral stationary column (Chiralpak IC-column, 20×250 mm, Flowrate at 17 ml/min) using as a mobile phase a mixture ofheptane/ethanol/trifluoroacetic acid (80/20/02) to yield 2.36 mg (0.05.4mmol, 1.6%) of enantiomer 1(Formula Ia-iii-e1) as an off-white solid and17.8 mg (0.041 mmol, yield 12%) of enantiomer 2 (Formula Ia-iii-e2) asan off-white soild. Both enantiomers were analyzed for enantiomericpurity by HPLC using Chiralpak IC-column (0.46×25) and as a mobile phasea mixture of heptane/ethanol/trifluoroacetic acid (80/20/02) at 0.7ml/min flow rate. The enantiomeric excess (ee) of the Enantiomer 1(Formula Ia-iii-e1) that was eluted at R_(t)=14.87 min was determined tobe 90.7% and Enantiomer 2 (Formula Ia-iii-e2) that was eluted atR_(t)18.51 min was 98.7%, respectively. LC-MS and The ¹H-NMR spectra forboth enantiomers are in accordance with the chemical structure. LC-MSLC-MS [M+H] 435 (C₂₂K₄N₂O₂S₃+H, requires 435.02).

Example 12 Preparation of2-((4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticAcid (Formula Ia-xix)

The reaction of 2-acetylthiophene (2.05 mL, 2.38 g, 18.9 mmol) andp-anisaldehyde (2.3 mL, 18.9 mmol) afforded chalcone(E)-3-(4-methoxyphenyl)-1-(thiophen-2-yl)prop-2-en-1-one with 89% yield(4.13 g, 16.9 mmol) as an off-white solid (Obtained by precipitation).The ¹H-NMR spectrum was in accordance with the chemical structure.

A mixture of chalcone(E)-3-(4-methoxyphenyl)-1-(thiophen-2-yl)prop-2-en-1-one (1.5 g, 6.1mmol), N-acetylglycinamide (850 mg, 7.3 mmol, 1.2 equiv.) and Cs₂CO₃(2.4 g, 7.3 mmol, 1.2 equiv.) in DMF (15 mL) was refluxed until TLCshowed complete conversion. After 1 d conversion was complete and themixture was poured into 3N HCl (50 mL). The mixture was extracted withCH₂Cl₂ (2×30 mL). The combined organic layers were washed with H₂O (100mL) and brine (100 ml) and dried over Na₂SO₄. The solvent was evaporatedin vacuo and the residue was taken up in CH₂Cl₂. A solid precipitatedand the filtrate was purified by automated column chromatography on theISCO-companion (SiO₂, gradient ethyl acetate/heptane) to give4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2(1H)-one (839 mg, 2.96mmol, 48%) as a brown solid. The ¹H-NMR spectrum was in accordance withthe chemical structure.

A mixture of 4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2(1H)-one (400mg, 1.41 mmol) and Lawesson's reagent (344 mg, 0.85 mmol) in THF (20 mL)was heated to reflux for 20 hours. It was concentrated and the residuewas purified by automated column chromatography on the ISCO-companion(SiO₂, gradient ethyl acetate/heptane) to give4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridine-2(1H)-thione (80 mg, 0.27mmol, 31%) as a brown solid.

Alkylation of compound4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridine-2(1H)-thione (80 mg, 0.27mmol) with alpha-bromophenylacetic acid following the general procedureafforded methyl2-((4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetate(75 mg, 0.17 mmol, 63%) as a tan solid.

Saponification of methyl2-((4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetate(75 mg, 0.17 mmol) following the general procedure afforded finalproduct2-((4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid (1.82 mg, 0.004 mmol, yield 3%) as a tan solid and with an HPLCpurity of 87.4%. LC-MS [M+H] 434 (C₂₄H₁₉NO₃S₂+H, requires 434.08). The¹H-NMR spectrum was in accordance with the chemical structure.

Example 13 Preparation of2-((3-cyano-6-(furan-2-yl)-4-(4-methoxyphenyl)pyridin-2-yl)thio)-2-phenylaceticAcid (Formula Ia-xx)

The reaction of 2-acetylfuran (1.57 mL, 18.9 mmol) and4-methoxybenzaldehyde (2.57 g, 18.9 mmol) afforded chalcone(E)-1-(furan-2-yl)-3-(4-methoxyphenyl)prop-2-en-1-one (3.67 g, 16.1mmol, yield 85%) as a yellow solid (purification by columnchromatography). The ¹H-NMR spectrum was in accordance with the chemicalstructure.

Reaction of chalcone(E)-1-(furan-2-yl)-3-(4-methoxyphenyl)prop-2-en-1-one (1.5 g, 6.6 mmol)with 1 equivalent 2-cyanothioacetamide afforded the desired thiopyridinederivative that was purified by silica gel chromatography. The pure6-(furan-2-yl)-4-(4-methoxyphenyl)-2-thioxo-1,2-dihydropyridine-3-carbonitrilewas obtained with a 34% yield (695 mg, 2.2 mmol) as an orange solid. The¹H-NMR spectrum was in accordance with the chemical structure.

Alkylation of6-(furan-2-yl)-4-(4-methoxyphenyl)-2-thioxo-1,2-dihydropyridine-3-carbonitrile(695 mg, 2.2 mmol) with methyl α-bromophenylacetate (343 mg, 0.25 mmol,1.1 equiv.) afforded methyl2-((3-cyano-6-(furan-2-yl)-4-(4-methoxyphenyl)pyridin-2-yl)thio)-2-phenylacetatein a 84% yield (870 mg, 1.9 mmol) as a brown solid. The ¹H-NMR spectrumwas in accordance with the chemical structure.

Saponification of methyl2-((3-cyano-6-(furan-2-yl)-4-(4-methoxyphenyl)pyridin-2-yl)thio)-2-phenylacetate(400 mg, 0.88 mmol) with 1N NaOH in THF-methanol mixture afforded finalproduct2-((3-cyano-6-(furan-2-yl)-4-(4-methoxyphenyl)pyridin-2-yl)thio)-2-phenylaceticacid (70 mg, 0.16 mmol, yield 18%) as a brown solid and with an HPLCpurity of 98.1%. LC-MS [M+H] 443.0 (C₂₅H₁₈N₂O₄S₂+H, requires 442.1). The¹H-NMR spectrum was in accordance with the chemical structure.

Example 14 Preparation of2-((3-cyano-6-(thiophen-2-yl)-4-(p-tolyl)pyridin-2-yl)thio)-2-phenylaceticAcid (Formula Ia-xxi)

The reaction of 2-acetylthiophene (2.05 mL, 2.38 g, 18.9 mmol) andp-tolylaldehyde (2.2 mL, 18.9 mmol) afforded chalcone(E)-1-(thiophen-2-yl)-3-(p-tolyl)prop-2-en-1-one (3.63 g, 15.9 mmol,84%) as an off-white solid (obtained by precipitation). The ¹H-NMRspectrum was in accordance with the chemical structure.

The reaction of chalcone(E)-1-(thiophen-2-yl)-3-(p-tolyl)prop-2-en-1-one (1.0 g, 4.38 mmol) with1 equivalent 2-cyanothioacetamide afforded the desired thiopyridinederivative that was purified by silica gel chromatography. The pure6-(thiophen-2-yl)-2-thioxo-4-(p-tolyl)-1,2-dihydro-pyridine-3-carbonitrilewas obtained with a 46% yield (620 mg, 2.0 mmol) as an orange solid. The¹H-NMR spectrum was in accordance with the chemical structure.

Alkylation of compound6-(thiophen-2-yl)-2-thioxo-4-(p-tolyl)-1,2-dihydro-pyridine-3-carbonitrile(331 mg, 1.07 mmol) with methyl α-bromophenylacetate (270 mg, 1.18 mmol,1.1 equiv.) afforded methyl2-((3-cyano-6-(thiophen-2-yl)-4-(p-tolyl)pyridin-2-yl)thio)-2-phenylacetatein a quantitative yield (515 mg, max. 1.07 mmol) as a brown solid. The¹H-NMR spectrum was in accordance with the chemical structure.

Saponification of methyl2-((3-cyano-6-(thiophen-2-yl)-4-(p-tolyl)pyridin-2-yl)thio)-2-phenylacetate(515 mg, 1.13 mmol) with 1N NaOH in THF-methanol mixture afforded finalproduct2-((3-cyano-6-(thiophen-2-yl)-4-(p-tolyl)pyridin-2-yl)thio)-2-phenylaceticacid (18.2 mg, 0.04 mmol, yield 4%) as a tan solid with an HPLC purityof 95.4%. LC-MS [M+H] 443.1 (C₂₅H₁₈N₂O₂S₂+H, requires 443.08). The¹H-NMR spectrum was in accordance with the chemical structure.

Example 15 Preparation of2-((3-cyano-4-(4-fluorophenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticAcid (Formula Ia-xxii)

The reaction of 2-acetylthiophene (2.05 mL, 2.38 g, 18.9 mmol) andp-fluorbenzaldehyde (2.35 g, 18.9 mmol) afforded chalcone(E)-3-(4-fluorophenyl)-1-(thiophen-2-yl)prop-2-en-1-one (4.03 g, 17.3mmol, 92%) as an off-white solid (obtained by precipitation). The ¹H-NMRspectrum was in accordance with the chemical structure.

The reaction of chalcone(E)-3-(4-fluorophenyl)-1-(thiophen-2-yl)prop-2-en-1-one with 1equivalent of 2-cyanothioacetamide afforded the desired4-(4-fluorophenyl)-6-(thiophen-2-yl)-2-thioxo-1,2-dihydropyridine-3-carbonitrilewith a 10% yield (136 mg, 0.44 mmol) as an orange solid, which was usedas such in the next reaction. The ¹H-NMR spectrum was in accordance withthe chemical structure.

Alkylation of4-(4-fluorophenyl)-6-(thiophen-2-yl)-2-thioxo-1,2-dihydropyridine-3-carbonitrile(136 mg, 0.44 mmol) with methyl α-bromophenylacetate (110 mg, 0.48 mmol,1.1 equiv.) afforded methyl2-((3-cyano-4-(4-fluorophenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetate(60 mg, 0.13 mmol, yield 30%) as a brown solid. The ¹H-NMR spectrum wasin accordance with the chemical structure.

Saponification of methyl2-((3-cyano-4-(4-fluorophenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetate(515 mg, 1.13 mmol) with 1N NaOH in a THF-methanol mixture afforded2-((3-Cyano-4-(4-fluorophenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid (18.17 mg, 0.04 mmol, yield 31%) as a tan solid with an HPLC purityof 98.5%. LC-MS [M+H] 447.1 (C₂₄H₁₅FN₂O₂S₂+H, requires 447.06). The¹H-NMR spectrum was in accordance with the chemical structure.

Example 16 Preparation of2-((4-(4-bromophenyl)-3-cyano-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticAcid (Formula Ia-xxiii)

The reaction of 2-acetylthiophene (2.05 mL, 2.38 g, 18.9 mmol) and4-bromobenzaldehyde (3.5 g, 18.9 mmol) afforded chalcone(E)-3-(4-bromophenyl)-1-(thiophen-2-yl)prop-2-en-1-one (4.99 g, 17.1mmol, 90%) as an off-white solid (Obtained by precipitation). The ¹H-NMRspectrum was in accordance with the chemical structure.

The reaction of chalcone(E)-3-(4-bromophenyl)-1-(thiophen-2-yl)prop-2-en-1-one (1.0 g, 3.4 mmol)with 1 equivalent 2-cyanothioacetamide afforded the desired4-(4-bromophenyl)-6-(thiophen-2-yl)-2-thioxo-1,2-dihydropyridine-3-carbonitrilewith a 12% yield ((152 mg, 0.41 mmol) as an orange solid which was usedas such in the next reaction. The ¹H-NMR spectrum was in accordance withthe chemical structure.

Alkylation of4-(4-bromophenyl)-6-(thiophen-2-yl)-2-thioxo-1,2-dihydropyridine-3-carbonitrile(152 mg, 0.41 mmol) with methyl α-bromophenylacetate (110 mg, 0.48 mmol,1.1 equiv.) afforded methyl2-(((4-(4-bromophenyl)-3-cyano-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetate(74 mg, 0.14 mmol, yield 35%) as a yellow solid. The ¹H-NMR spectrum wasin accordance with the chemical structure.

Saponification of methyl2-((4-(4-bromophenyl)-3-cyano-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetate(74 mg, 0.14 mmol) with 1N NaOH in THF-methanol mixture afforded2-(((4-(4-bromophenyl)-3-cyano-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid (0.4 mg, 0.8 μmol, yield 0.6%) as a tan solid with an HPLC purityof 81%. LC-MS [M+H] 507/509 (C₂₄H₁₅BrN₂O₂S₂+H, requires 506.98/508.98).The ¹H-NMR spectrum was in accordance with the chemical structure.

Example 17 Preparation of2-((3-cyano-6-(furan-2-yl)-4-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticAcid (Formula Ia-xxiv)

The reaction of 2-acetylthiophene (2.5 g, 19.8 mmol) and 2-furaldehyde(1.9 g, 19.8 mmol) afforded chalcone(E)-3-(furan-2-yl)-1-(thiophen-2-yl)prop-2-en-1-one (3.66 g, 17.9 mmol,90%) as an orange oil, which solidified overnight (purification bycolumn chromatography). The ¹H-NMR spectrum was in accordance with thechemical structure.

The reaction of chalcone(E)-3-(furan-2-yl)-1-(thiophen-2-yl)prop-2-en-1-one (2.8 g, 13.7 mmol)with 1 equivalent 2-cyanothioacetamide afforded the desired6-(Furan-2-yl)-4-(thiophen-2-yl)-2-thioxo-1,2-dihydropyridine-3-carbonitrilewith a 22% yield (863 mg, 3.0 mmol) as an orange solid. The ¹H-NMRspectrum was in accordance with the chemical structure.

Alkylation of6-(furan-2-yl)-4-(thiophen-2-yl)-2-thioxo-1,2-dihydropyridine-3-carbonitrilewith (863 mg, 3.0 mmol) methyl α-bromophenylacetate (765 mg, 3.3 mmol,1.1 equiv.) afforded methyl2-((3-cyano-6-(furan-2-yl)-4-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetate(1.3 g, 3.0 mmol, yield 99%) as a yellow solid. The ¹H-NMR spectrum wasin accordance with the chemical structure.

Saponification of methyl2-((3-cyano-6-(furan-2-yl)-4-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetate(392 mg, 0.91 mmol) with 1N NaOH in THF-methanol mixture afforded2-((3-Cyano-6-(furan-2-yl)-4-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid (112.11 mg, 0.27 mmol, yield 30%) as a tan solid with as a greysolid with an HPLC purity of 96.2%. LC-MS [M+H] 419 (C₂₂H₁₄N₂O₃S₂+H,requires 419.04). The ¹H-NMR spectrum was in accordance with thechemical structure.

Example 18 Preparation of2-((3-cyano-4,6-di(furan-2-yl)pyridin-2-yl)thio)-2-phenylacetic Acid(Formula Ia-xxv)

The reaction of furylmethylketone (2.5 g, 22.7 mmol) and 2-furaldehyde(2.2 g, 22.7 mmol) afforded chalcone(E)-1,3-di(furan-2-yl)prop-2-en-1-one (3.33 g, 17.7 mmol, yield 78%) asan yellow solid (obtained by precipitation). The ¹H-NMR spectrum was inaccordance with the chemical structure.

The reaction of chalcone (E)-1,3-di(furan-2-yl)prop-2-en-1-one (1.75 g,9.3 mmol) with 1 equivalent 2-cyanothioacetamide afforded the desired4,6-Di(furan-2-yl)-2-thioxo-1,2-dihydropyridine-3-carbonitrile with a29% yield (720 mg, 2.7 mmol) as an orange solid. The ¹H-NMR spectrum wasin accordance with the chemical structure.

Alkylation of4,6-di(furan-2-yl)-2-thioxo-1,2-dihydropyridine-3-carbonitrile (1.5mmol) with methyl α-bromophenylacetate (1.7 mmol, 1.1 equiv.) affordedthe desired methyl2-((3-cyano-4,6-di(furan-2-yl)pyridin-2-yl)thio)-2-phenylacetate in a80% yield that was used as is in the next step.

Saponification of methyl2-((3-cyano-4,6-di(furan-2-yl)pyridin-2-yl)thio)-2-phenylacetate (500mg, 1.2 mmol) with 1N NaOH in THF-methanol mixture afforded2-((3-cyano-4,6-di(furan-2-yl)pyridin-2-yl)thio)-2-phenylacetic acid(191 mg, 0.47 mmol, yield 40%) as a grey solid with an HPLC purity of97.8%. LC-MS [M+H] 403.1 (C₂₂H₁₄N₂O₄S+H, requires 403.07). The ¹H-NMRspectrum was in accordance with the chemical structure.

Example 19 Preparation of2-((3-cyano-4-(furan-2-yl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticAcid (Formula Ia-xxxii)

The reaction of 2-acetylthiophene (2.5 g, 19.8 mmol) and 2-furaldehyde(1.9 g, 19.8 mmol) afforded chalcone(E)-3-(furan-2-yl)-1-(thiophen-2-yl)prop-2-en-1-one (3.66 g, 17.9 mmol,yield 90%) as an orange oil, which solidified overnight (purification bycolumn chromatography). The ¹H-NMR spectrum was in accordance with thechemical structure.

The reaction of chalcone(E)-3-(furan-2-yl)-1-(thiophen-2-yl)prop-2-en-1-one (3.66 g, 17.9 mmol)with 1 equivalent 2-cyanothioacetamide afforded the desired4-(Furan-2-yl)-6-(thiophen-2-yl)-2-thioxo-1,2-dihydropyridine-3-carbonitrilewith a 39% yield (2.0 g, 7.0 mmol) as an orange solid. The ¹H-NMRspectrum was in accordance with the chemical structure.

Alkylation of4-(furan-2-yl)-6-(thiophen-2-yl)-2-thioxo-1,2-dihydropyridine-3-carbonitrilewith (1.0 mmol) with methyl α-bromophenylacetate (1.1 mmol, 1.1 equiv.)afforded the desired methyl2-((3-cyano-4-(furan-2-yl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacetate in a 76% yield.

Saponification of methyl2-((3-cyano-4-(furan-2-yl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacetate (319 mg, 0.76 mmol) with 1N NaOH in THF-methanol mixtureafforded2-((3-cyano-4-(furan-2-yl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid (94.9 mg, 0.227 mmol, yield 30%) as a grey solid with an HPLCpurity of 96.9%. LC-MS [M+H] 419 (C₂₂H₁₄N₂O₃S₂+H, requires 419.04). The¹H-NMR spectrum was in accordance with the chemical structure.

Example 20 Preparation of2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)butanoicAcid (Formula Ia-xxix)

The reaction of 2-acetylthiophene (2.05 mL, 2.38 g, 18.9 mmol) andp-anisaldehyde (2.3 mL, 18.9 mmol) afforded chalcone(E)-3-(4-methoxyphenyl)-1-(thiophen-2-yl)prop-2-en-1-one (4.13 g, 16.9mmol, 89%) as an off-white solid (obtained by precipitation).

The reaction of chalcone4-(4-methoxyphenyl)-6-(thiophen-2-yl)-2-thioxo-1,2-dihydropyridine-3-carbonitrile(1.5 g, 6.1 mmol) with 1 equivalent 2-cyanothioacetamide afforded thedesired4-(4-methoxyphenyl)-6-(thiophen-2-yl)-2-thioxo-1,2-dihydropyridine-3-carbonitrilewith a 24% yield (470 mg, 1.4 mmol) as an orange solid. The ¹H-NMRspectrum was in accordance with the chemical structure.

Alkylation of4-(4-methoxyphenyl)-6-(thiophen-2-yl)-2-thioxo-1,2-dihydropyridine-3-carbonitrile(200 mg, 0.62 mmol) with 2-bromobutyric acid methyl ester (0.68 mmol,1.1 equiv.) afforded the desired methyl2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)butanoate(221 mg, 0.52 mmol, yield 76%) as a yellow solid. The ¹H-NMR spectrumwas in accordance with the chemical structure.

Saponification of methyl2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)butanoate(221 mg, 0.50 mmol) with 1N NaOH in THF-methanol mixture afforded thecrude desired product that was purified by preparative HPLCchromatography. The purified2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)butanoicacid (68.9 mg, 0.17 mmol) was obtained in 32% yield as an off-whitesolid with an HPLC purity of 95.2%. LC-MS [M+H] 411.0 (C₂₁H₁₈N₂O₃S₂+H,requires 411.08). The ¹H-NMR spectrum was in accordance with thechemical structure.

Example 21 Preparation of2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetamide(Formula Ib-ii)

A mixture of methyl2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetate(prepared as described in Example 4) (100 mg, 0.212 mmol) and 7N NH₃ inmethanol (10 mL) was stirred at 50° C. in a pressure tube for 2 days.The mixture was concentrated and triturated with ethyl acetate to yieldfinal product2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetamide(30 mg, 0.065 mmol, yield 31%) as a tan solid with an HPLC purity of97.0%. LC-MS [M+H] 458.1 (C₂₅H₁₉N₃O₂S₂+H, requires 458.09). The ¹H-NMRspectrum was in accordance with the chemical structure.

Example 22 Preparation of2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-N-hydroxy-2-phenylacetamide(Formula Ib-iii)

A mixture of methyl2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetate(prepared as described in Example 4) (100 mg, 0.212 mmol), 50% aqueousNH₂OH (1.0 mL), 1M NaOH (0.41 mL, 0.42 mmol) in THF (1 mL) was stirredfor 3 days at room temperature. The mixture was diluted with H₂O (3 mL)and extracted with ethyl acetate (2×10 mL). The combined organic layerswere dried over Na₂SO₄ and the solvent evaporated in vacuo. The residuewas purified by preparative HPLC (reversed phase, acetonitrile, aqueous(NH₄)HCO₃) and the product fractions were lyophilized to give thedesired2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-N-hydroxy-2-phenylacetamide(50 mg, 0.106 mmol, 50%) as a fluffy off-white solid with an HPLC purityof 97.3%. LC-MS [M+H] 474.0 (C₂₅H₁₉N₃O₃S₂+H, requires 474.09). The¹H-NMR spectrum was in accordance with the chemical structure.

Example 23 Preparation of2-((2-hydroxy-1-phenylethyl)thio)-4-(4-methoxyphenyl)-6-(thiophen-2-yl)nicotinonitrile(Formula IIb-i)

A mixture of4-(4-methoxyphenyl)-6-(thiophen-2-yl)-2-thioxo-1,2-dihydropyridine-3-carbonitrile(prepared as described in Example 4) (156 mg, 0.48 mmol), K₂CO₃ (73 mg,0.528mmol, 1.1 equiv.) and 2-bromo-2-phenyl-ethanol (107 mg, 0.53 mmol,1.1 equiv.) in acetone was refluxed for 3 hours. After cooling to roomtemperature, the mixture was filtered and the solvent was evaporated invacuo. Purification by repeated automated column chromatography on theISCO-companion (SiO₂, gradient ethyl acetate/heptane) gave2-((2-hydroxy-1-phenylethyl)thio)-4-(4-methoxyphenyl)-6-(thiophen-2-yl)nicotinonitrile(135 mg, 0.30 mmol, yield 63%) as an off-white solid with an HPLC purityof 97.4%. LC-MS [M+H] 445 (C₂₅H₂₀N₂O₂S₂+H, requires 445.1). The ¹H-NMRspectrum was in accordance with the chemical structure.

Example 24 Preparation of2-((3-cyano-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylaceticAcid (Formula Ia-xii)

A mixture of thiophene-2-carboxaldehyde (0.93 mL, 1.12 g, 10.0 mmol),2-cyanothioacetamide (1.0 g, 10.0 mmol) and 2 drops of NEt₃ (12 mL) wasrefluxed for 25 min. The mixture was cooled to room temperature andfiltered. The solid was washed with ethanol (20 mL) and dried in air togive the desired alkene as yellow crystals (1.5 g, 7.7 mmol, 77%). Amixture of these crystals, cyclohexanone (0.88 mL, 833 mg, 8.5 mmol, 1.1equiv.) and 3 drops of piperidine in ethanol (50 mL) was refluxed for 3hours. It was concentrated in vacuo until ˜25 mL of solvent were left.The mixture was cooled to room temperature and left for ˜2 h. Theresulting solid was filtered off, washed with ethanol (10 mL) andheptane (50 mL) and dried in air to give2-mercapto-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinoline-3-carbonitrile(586 mg, 2.15 mmol, 28%) as an orange solid. The ¹H-NMR spectrum was inaccordance with the chemical structure.

A mixture of2-mercapto-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinoline-3-carbonitrile(272 mg, 1.0 mmol), K₂CO₃ (152 mg, 1.1 mmol) and methylα-bromophenylacetate (229 mg, 1.0 mmol) in acetone (15 mL) was refluxedfor 2 hours. The mixture was cooled to room temperature and filtered.The solvent was removed in vacuo and the residue was purified byautomated column chromatography on the ISCO-companion (SiO₂, gradientethyl acetate/heptane) to give methyl2-((3-cyano-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylacetate(276 mg, 0.66 mmol, 65%) as a yellowish solid. The ¹H-NMR spectrum wasin accordance with the chemical structure.

A mixture of methyl2-((3-cyano-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylacetate(276 mmol, 0.656 mmol) in THF (2 mL), methanol (2 mL) and 2N NaOH (2 mL)was stirred for 2 hours at room temperature. After completion of thereaction, the organic solvent was removed in vacuo and the aqueousresidue was diluted with H₂O (5 mL). The pH was adjusted to 5 byaddition of 1M HCl. The solid was filtered off, washed with H₂O (3×10mL) and dried in air to give the crude2-((3-cyano-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylaceticacid as a tan solid.

The racemic acid product was separated into enantiomers by preparativeHPLC on a chiral stationary column (Chiralpak IC-column, 20×250 mm, Flowrate at 17 ml/min) using as a mobile phase a mixture ofheptane/ethanol/trifluoroacetic acid (80/20/02) to yield (73.6 mg, 0.18mmol, 28%) of enantiomer 1 (Formula Ia-xii-e1) as an off-white solid and(97.2 mg, 0.24 mmol, 36%) of enantiomer 2 (Formula Ia-xii-e2) as anoff-white soild. Both enantiomers were analyzed for enantiomeric purityby HPLC using Chiralpak IC-column (0.46×25) and as a mobile phase amixture of heptane/ethanol/trifluoroacetic acid (80/20/02) at 0.7 ml/minflow rate. The enantiomeric excess (ee) of the Enantiomer 1(FormulaIa-xii-e1) that was eluted at R_(t)=14.18 min was determined to be 72.1%and Enantiomer 2 (Formula Ia-xii-e2) that was eluted at R_(t)=18.18 minwas 65.8%, respectively. LC-MS and the ¹H-NMR spectra for bothenantiomers are in accordance with the chemical structure. LC-MS LC-MS[M+H] 407 (C₂₂H₁₈N₂O₂S₂+H, requires 407.08).

Example 25 Preparation of2-((3-cyano-4-phenyl-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylaceticAcid (Formula Ia-xvii)

A mixture of benzaldehyde (605 mg, 5.7 mmol), malononitrile (376 mg, 5.7mmol), 2-cyanothioacetamide (570 mg, 5.7 mmol) and three drops ofpiperidine in ethanol (25 mL) was refluxed for 5 hours. H₂O (25 mL) wasadded and the solid was filtered off and washed with H₂O (2×50 ml) anddried in air to give2,6-diamino-4-phenyl-4H-thiopyran-3,5-dicarbonitrile (1.12 g, 4.4 mmol,77%) as a tan solid. The ¹H-NMR spectrum was in accordance with thechemical structure.

A mixture of 2,6-diamino-4-phenyl-4H-thiopyran-3,5-dicarbonitrile (1.12g, 4.4 mmol) and 4-(1-cyclohexen-1-yl)morpholine (0.71 mL, 721 mg, 4.4mmol) in ethanol (50 mL) was refluxed for 2 hours. The mixture wascooled to room temperature and the pH was adjusted to 5 by addition of6M HCl. The mixture was stirred overnight at room temperature,concentrated to half-volume in vacuo and filtered. H₂O (25 mL) was addedand the resulting solid was washed with H₂O (25 mL), acetic acid (25 mL)and heptane (50 mL) and dried in air to give a yellow solid.Recrystallization from acetic acid (10 mL) gave, after filtration,washing with acetic acid (5 mL) and heptane (25 mL) and drying in air,2-mercapto-4-phenyl-5,6,7,8-tetrahydroquinoline-3-carbonitrile (325 mg,1.21 mmol, 28%) as a yellow solid. The ¹H-NMR spectrum was in accordancewith the chemical structure.

A mixture of2-mercapto-4-phenyl-5,6,7,8-tetrahydroquinoline-3-carbonitrile (266 mg,1.0 mmol), K₂CO₃ (152 mg, 1.1 mmol) and methyl α-bromophenylacetate (229mg, 1.0 mmol) in acetone (15 mL) was refluxed for 2 hours. The mixturewas cooled to room temperature and filtered. The solvent was removed invacuo and the residue was purified by automated column chromatography onthe ISCO-companion (SiO₂, gradient ethyl acetate/heptane) to give methyl2-((3-cyano-4-phenyl-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylacetate(276 mg, 0.66 mmol, yield 65%) as a yellowish solid. The ¹H-NMR spectrumwas in accordance with the chemical structure.

A mixture of methyl2-((3-cyano-4-phenyl-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylacetate(280 mg, 0.67 mmol) in THF (2 mL), methanol (2 mL) and 2M LiOH (2 mL)was stirred for 2 hours at room temperature. After completion of thereaction, the solvent was removed in vacuo and the residue was stirredin ethyl acetate (10 mL). The solid was filtered and washed with ethylacetate (3×5 mL) and dried in air. It was dissolved in H₂O (5 mL) andthe pH of the solution was adjusted to 5 by addition of 1M HCl. Theresulting solid was filtered and washed with H₂O (3×10 mL) and dried inair to give the desired2-((3-Cyano-4-phenyl-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylaceticacid (150 mg, 0.375 mmol, yield 6%) as an off-white solid with an HPLCpurity of 99.5%. LC-MS [M+H] 401 (C₂₄H₂₀N₂O₂S+H, requires 401.12). The¹H-NMR spectrum was in accordance with the chemical structure.

Example 26 Preparation of2-((4-(4-chlorophenyl)-3-cyano-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylaceticAcid (Formula Ia-xviii)

A mixture of 4-chlorobenzaldehyde (562 mg, 5.0 mmol), malononitrile (330mg, 5.0 mmol), 2-cyanothioacetamide (500 mg, 5.0 mmol) and three dropsof piperidine in ethanol (25 mL) was refluxed for 5 hours. H₂O (25 mL)was added and the solid was filtered off and washed with H₂O (2×50 ml)and dried in air to give2,6-diamino-4-(4-chlorophenyl)-4H-thiopyran-3,5-dicarbonitrile (1.07 g,3.8 mmol, 76%) as a yellow solid. The ¹H-NMR spectrum was in accordancewith the chemical structure.

A mixture of2,6-diamino-4-(4-chlorophenyl)-4H-thiopyran-3,5-dicarbonitrile (1.07 g,3.7 mmol) and 4-(1-cyclohexen-1-yl)morpholine (0.62 mL, 620 mg, 3.7mmol) in ethanol (25 mL) was refluxed for 2 hours. The mixture wascooled to room temperature and the pH was adjusted to 5 by addition of6M HCl. The mixture was stirred overnight at room temperature,concentrated to half-volume in vacuo and filtered. The solid was washedwith H₂O (25 mL) and heptane (50 mL) and dried in air to give an orangesolid. Recrystallization from acetic acid (10 mL) gave, afterfiltration, washing with acetic acid (5 mL) and heptane (25 mL) anddrying in air, compound2-mercapto-4-(4-chlorophenyl)-5,6,7,8-tetrahydroquinoline-3-carbonitrile(325 mg, 1.08 mmol, yield 29%) as a yellow solid. The ¹H-NMR spectrumwas in accordance with the chemical structure.

A mixture of2-mercapto-4-phenyl-5,6,7,8-tetrahydroquinoline-3-carbonitrile (300 mg,1.0 mmol), K₂CO₃ (152 mg, 1.1 mmol) and methyl α-bromophenylacetate (229mg, 1.0 mmol) in acetone (15 mL) was refluxed for 2 hours. The mixturewas cooled to room temperature and filtered. The solvent was removed invacuo to give the desired methyl2-((3-cyano-4-(4-chlorophenyl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylacetate(463 mg, 1.0 mmol, yield 100%) as a as a brownish foam, that was used inthe next step without further purification. The ¹H-NMR spectrum was inaccordance with the chemical structure.

A mixture of methyl2-((3-cyano-4-(4-chlorophenyl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylacetate(463 mg, 1.0 mmol) in THF (2 mL), methanol (2 mL) and 2M NaOH (2 mL) wasstirred for 3 hours at room temperature. After completion of thereaction, the organic solvent was removed in vacuo and the aqueousresidue was diluted with H₂O (5 mL). The pH was adjusted to 5 byaddition of 1M HCl. The solid was filtered off, washed with H₂O (3×10mL) and dried in air to give the crude acid as a tan solid. Purificationby repeated automated column chromatography on the ISCO-companion (SiO₂,gradient CH₂Cl₂/methanol) gave2-((4-(4-Chlorophenyl)-3-cyano-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylaceticacid (61 mg, 0.14 mmol, yield 14%) as a pinkish foam with an HPLC purityof 99.8%. LC-MS [M+H] 435 (C₂₄H₁₉ClN₂O₂S+H, requires 435.09). The ¹H-NMRspectrum was in accordance with the chemical structure.

Example 27 Preparation of2-((3-cyano-4-(4-methoxyphenyl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylaceticAcid (Formula Ia-xxvi)

A mixture of p-anisaldehyde (681 mg, 5.0 mmol), malononitrile (330 mg,5.0 mmol), 2-cyanothioacetamide (500 mg, 5.0 mmol) and three drops ofpiperidine in ethanol (25 mL) was refluxed for 5 hours. H₂O (25 mL) wasadded and the solid was filtered off and washed with H₂O (2×50 ml) anddried in air to give2,6-diamino-4-(4-methoxyphenyl)-4H-thiopyran-3,5-dicarbonitrile (570 mg,2.0 mmol, yield 40%) as a tan solid. The ¹H-NMR spectrum was inaccordance with the chemical structure.

A mixture of2,6-diamino-4-(4-methoxyphenyl)-4H-thiopyran-3,5-dicarbonitrile (570 mg,1.97 mmol) and 4-(1-cyclohexen-1-yl)morpholine (0.32 mL, 330 mg, 1.97mmol) in ethanol (10 mL) was refluxed for 2 hours. The mixture wascooled to room temperature and the pH was adjusted to 5 by addition of6M HCl. The mixture was stirred for 2 d at room temperature andfiltered. The solid was washed with H₂O (25 mL) and heptane (50 mL) anddried in air to give the desired2-mercapto-4-(4-methoxyphenyl)-5,6,7,8-tetrahydroquinoline-3-carbonitrile(210 mg, 0.7 mmol, yield 35%) as a yellow solid. The ¹H-NMR spectrum wasin accordance with the chemical structure.

Alkylation of2-mercapto-4-(4-methoxyphenyl)-5,6,7,8-tetrahydroquinoline-3-carbonitrile(210 mg, 0.71 mmol) with methyl alpha-bromophenylacetate (0.78 mmol, 1.1eq) in presence of K₂CO₃ in acetone gave compound the desired product asa colorless oil, after purification by automated column chromatographyon the ISCO-companion (SiO₂, gradient ethyl acetate/heptane). Additionalpurification was achieved by trituration from methanol (2 mL).Filtration of the solid, washing with a small volume of methanol (1 mL)and drying in air afforded methyl2-((3-cyano-4-(4-methoxyphenyl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylacetate(160 mg, 0356 mmol, yield 50%) as a white solid. The ¹H-NMR spectrum wasin accordance with the chemical structure.

A mixture of methyl2-((3-cyano-4-(4-methoxyphenyl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylacetate(288 mg, 0.65 mmol) in THF (2 mL), methanol (2 mL) and 2M NaOH (1.3 mL)was stirred for 18 hours at room temperature. After completion of thereaction, the solvent was removed in vacuo and the residue was stirredin ethyl acetate (10 mL). The solid was filtered and washed with ethylacetate (3×5 mL) and dried in air. It was dissolved in H₂O (5 mL) andthe pH of the solution was adjusted to 5 by addition of 1M HCl. Theresulting solid was filtered and washed with H₂O (3×10 mL) and dried inair to give2-((3-Cyano-4-(4-methoxyphenyl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylaceticacid (125 mg, 0.29 mmol, yield 45%) as an off-white solid as an of withan HPLC purity of 99.9%. LC-MS [M+H] 431 (C₂₅H₂₂N₂O₃S+H, requires431.14). The ¹H-NMR spectrum was in accordance with the chemicalstructure.

Example 28 Preparation of2-((3-cyano-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinolin-2-yl)oxy)-2-phenylaceticAcid (Formula Ia-xxvii)

A mixture of thiophene-2-carboxaldehyde (1.9 mL, 2.24 g, 20 mmol), ethylcyanoacetate (2.1 mL, 2.26 g, 20 mmol) and 3 drops of piperidine inethanol (30 mL) was stirred for 2 hours. The solid was filtered off,washed with a little ethanol and dried in air to give (E)-ethyl2-cyano-3-(thiophen-2-yl)acrylate (3.1 g, 14.9 mmol, 75%) as off-whitecrystals.

A mixture of (E)-ethyl 2-cyano-3-(thiophen-2-yl)acrylate (1.5 g, 7.2mmol), cyclohexanone (0.75 mL, 710 mg, 7.2 mmol), NH₄OAc (210 mg, 3.65mmol) in ethanol (10 mL) was refluxed overnight. The mixture was cooledto room temperature and the resulting solid was filtered off, washedwith some ethanol (2 mL) and dried in air to give2-hydroxy-4-(thiophen-2-yl)-5,6,7,8-tetrahydro-quinoline-3-carbonitrile(70 mg, 0.27 mmol, 3.8%) as a yellow solid.

A mixture of2-hydroxy-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinoline-3-carbonitrile(70 mg, 0.27 mmol), K₂CO₃ (56 mg, 0.405 mmol) and methylα-bromophenylacetate (62 mg, 0.27 mmol) in acetone (10 mL) was refluxedfor 18 hours. The mixture was cooled to room temperature and filtered.The solvent was removed in vacuo and the residue was purified byautomated column chromatography on the ISCO-companion (SiO₂, gradientethyl acetate/heptane) to give methyl2-((3-cyano-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinolin-2-yl)oxy)-2-phenylacetate(60 mg, 0.148 mmol, 55%) as a white solid.

A mixture of methyl2-((3-cyano-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinolin-2-yl)oxy)-2-phenylacetate(60 mmol, 0.148 mmol) in THF (1 mL), methanol (1 mL) and 2M NaOH (1 mL)was stirred for 2 hours at room temperature. After completion of thereaction, the solvents were removed in vacuo and the solid residue wasstirred in ethyl acetate (10 mL). The solid was filtered off and thefiltrate was concentrated in vacuo and taken up in H₂O (5 mL). The pHwas adjusted to 5 by addition of 1M HCl. The solid was filtered off,washed with H₂O (3×10 mL) and dried in air to give2-((3-cyano-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinolin-2-yl)oxy)-2-phenylaceticacid (50 mg, 0128 mmol, yield 87%) as an off-white solid with an HPLCpurity of 96.5%. LC-MS [M+H] 391 (C₂₂H₁₈N₂O₃S+H, requires 391.1). The¹H-NMR spectrum was in accordance with the chemical structure.

Example 29 Preparation of2-((3-cyano-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylacetamide(Formula Ib-i)

A mixture of methyl2-((3-cyano-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylacetate(prepared as described in Example 18) (124 mg, 0.29 mmol) in 7N NH₃ inmethanol (10 mL) was stirred for 3 d at room temperature. After 3 d themixture had become clear and the solvent was evaporated in vacuo. Theresidue was stirred in ethyl acetate (5 mL) and filtered, washed with alittle ethyl acetate (5 mL) and dried in air to give2-((3-cyano-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylacetamide(25 mg, 0.062 mmol, 21%) as a yellowish solid with an HPLC purity of96.3%. LC-MS [M+H] 406 (C₂₂H₁₉N₃OS₂+H, requires 406.1). The ¹H-NMRspectrum was in accordance with the chemical structure.

Example 30 Preparation of2-((2-hydroxy-1-phenylethyl)thio)-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinoline-3-carbonitrile(Formula IIb-ii)

A mixture of thiophene-2-carboxaldehyde (0.93 mL, 1.12 g, 10.0 mmol),2-cyanothioacetamide (1.0 g, 10.0 mmol) and 2 drops of triethylamine(NEt₃) (12 mL) was refluxed for 25 min. The mixture was cooled to roomtemperature and filtered. The solid was washed with ethanol (20 mL) anddried in air to give the alkene as yellow crystals (1.5 g, 7.7 mmol,77%). A mixture of these crystals, cyclohexanone (0.88 mL, 833 mg, 8.5mmol, 1.1 equiv.) and 3 drops of piperidine in ethanol (50 mL) wasrefluxed for 3 hours. It was concentrated in vacuo until ˜25 mL ofsolvent were left. The mixture was cooled to room temperature and leftfor ˜2 h. The resulting solid was filtered off, washed with ethanol (10mL) and heptane (50 mL) and dried in air to give2-mercapto-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinoline-3-carbonitrile(586 mg, 2.15 mmol, 28%) as an orange solid.

A mixture of2-mercapto-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinoline-3-carbonitrile(100 mg, 0.367 mmol), K₂CO₃ (56 mg, 0.404 mmol, 1.1 equiv.) and2-bromo-2-phenylethanol (74 mg, 0.367 mmol) in acetone was refluxed for3 hours. After cooling to room temperature, the mixture was filtered andthe solvent was evaporated in vacuo. Purification by repeated automatedcolumn chromatography on the ISCO-companion (SiO₂, gradient ethylacetate/heptane) gave2-((2-hydroxy-1-phenylethyl)thio)-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinoline-3-carbonitrile(73 mg, 0.186 mmol, yield 51%) as a yellow solid with an HPLC purity of95.3%. LC-MS [M+H] 393 (C₂₂H_(2O)N₂OS₂+H, requires 393.1). The ¹H-NMRspectrum was in accordance with the chemical structure.

When introducing elements of the present disclosure, the articles “a”,“an”, “the” and “said” are intended to mean that there are one or moreof the elements. The terms “comprising”, “including” and “having” areintended to be inclusive and mean that there may be additional elementsother than the listed elements.

In view of the above, it will be seen that the several objects of theinvention are achieved and other advantageous results attained.

As various changes could be made in the above products and methodswithout departing from the scope of the invention, it is intended thatall matter contained in the above description shall be interpreted asillustrative and not in a limiting sense.

What is claimed is:
 1. A method of controlling fungal pathogens, themethod comprising administering to a plant, a seed or soil a compositioncomprising an effective amount of a compound of Formula I or a saltthereof,

wherein R¹ is selected from the group consisting of OH and N(R⁷R⁸),wherein R⁷ and R⁸ are independently selected from the group consistingof hydrogen, OH, and CH₃; R² is selected from the group consisting ofalkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl, each of whichmay be optionally substituted with one or more substituents selectedfrom the group consisting of halogen, CH₃, OCH₃, CF₃, OCF₃, and CN; R³is selected from the group consisting of hydrogen, CN, ethynyl,CH₂N(R⁹R¹⁰), and C(O)N(R⁹R¹⁰), wherein R⁹ and R¹⁰ are each independentlyselected from the group consisting of hydrogen and alkyl; R⁴ is selectedfrom the group consisting of haloalkyl, aryl, arylalkyl, heteroaryl, andheteroarylalkyl, each of which may be optionally independentlysubstituted with one or more substituents selected from the groupconsisting of halogen, alkyl, alkoxy, haloalkyl, haloalkoxy, alkenyl,hydroxyalkyl, hydroxyl, N(R⁹R¹⁰), NR¹¹C(O)R¹², and O(CO)R¹³, wherein R⁹and R¹⁰ are independently selected from the group consisting of hydrogenand alkyl, R¹¹ is selected from the group consisting of hydrogen andalkyl, R¹² is alkyl, and R¹³ is alkyl; R⁵ is selected from the groupconsisting of hydrogen and alkyl; or R⁴ and R⁵ together form a fusedcycloalkyl or heterocycloalkyl ring having from 5 to 6 ring atomsselected from the group consisting of carbon, nitrogen, and oxygen; R⁶is selected from the group consisting of alkyl, haloalkyl, aryl,arylalkyl, heteroaryl, and heteroarylalkyl, each of which may beoptionally independently substituted with one or more substituentsselected from the group consisting of halogen, alkyl, alkoxy, haloalkyl,and haloalkoxy; or R⁵ and R⁶ together form a fused cycloalkyl orheterocycloalkyl ring having from 5 to 6 ring atoms selected from thegroup consisting of carbon, nitrogen, and oxygen; and E is selected fromthe group consisting of S, O, N(H), N(CH₃), and CH₂.
 2. The method ofclaim 1 wherein the compound is of Formula Ia or a salt thereof,

wherein R² is selected from the group consisting of alkyl, cycloalkyl,heterocycloalkyl, aryl and heteroaryl, each of which may be optionallyindependently substituted with one or more substituents selected fromthe group consisting of halogen, CH₃, OCH₃, CF₃, OCF₃, and CN; R³ isselected from the group consisting of hydrogen, CN, ethynyl,CH₂N(R⁹R¹⁰), and C(O)N(R⁹R¹⁰), wherein R⁹ and R¹⁰ are each independentlyselected from the group consisting of hydrogen and alkyl; R⁴ is selectedfrom the group consisting of haloalkyl, aryl, arylalkyl, heteroaryl, andheteroarylalkyl, each of which may be optionally independentlysubstituted with one or more substituents selected from the groupconsisting of halogen, alkyl, alkoxy, haloalkyl, haloalkoxy, alkenyl,hydroxyalkyl, hydroxyl, N(R⁹R¹⁰), NR¹¹C(O)R¹², and O(CO)R¹³, wherein R⁹and R¹⁰ are independently selected from the group consisting of hydrogenand alkyl, R¹¹ is selected from the group consisting of hydrogen andalkyl, R¹² is alkyl, and R¹³ is alkyl; R⁵ is selected from the groupconsisting of hydrogen and alkyl; or R⁴ and R⁵ together form a fusedcycloalkyl or heterocycloalkyl ring having from 5 to 6 ring atomsselected from the group consisting of carbon, nitrogen, and oxygen; R⁶is selected from the group consisting of alkyl, haloalkyl, aryl,arylalkyl, heteroaryl, and heteroarylalkyl, each of which may beoptionally independently substituted with one or more substituentsselected from the group consisting of halogen, alkyl, alkoxy, haloalkyl,and haloalkoxy; or R⁵ and R⁶ together form a fused cycloalkyl orheterocycloalkyl ring having from 5 to 6 ring atoms selected from thegroup consisting of carbon, nitrogen, and oxygen; and E is selected fromthe group consisting of S, O, N(H), N(CH₃), and CH₂.
 3. The method ofclaim 1 wherein the compound is of Formula Ib or a salt thereof,

wherein R² is selected from the group consisting of alkyl, cycloalkyl,heterocycloalkyl, aryl and heteroaryl, each of which may be optionallyindependently substituted with one or more substituents selected fromthe group consisting of halogen, CH₃, OCH₃, CF₃, OCF₃, and CN; R³ isselected from the group consisting of hydrogen, CN, ethynyl,CH₂N(R⁹R¹⁰), and C(O)N(R⁹R¹⁰), wherein R⁹ and R¹⁰ are each independentlyselected from the group consisting of hydrogen and alkyl; R⁴ is selectedfrom the group consisting of haloalkyl, aryl, arylalkyl, heteroaryl, andheteroarylalkyl, each of which may be optionally independentlysubstituted with one or more substituents selected from the groupconsisting of halogen, alkyl, alkoxy, haloalkyl, haloalkoxy, alkenyl,hydroxyalkyl, hydroxyl, N(R⁹R¹⁰), NR¹¹C(O)R¹², and O(CO)R¹³, wherein R⁹and R¹⁰ are independently selected from the group consisting of hydrogenand alkyl, R¹¹ is selected from the group consisting of hydrogen andalkyl, R¹² is alkyl, and R¹³ is alkyl; R⁵ is selected from the groupconsisting of hydrogen and alkyl; or R⁴ and R⁵ together form a fusedcycloalkyl or heterocycloalkyl ring having from 5 to 6 ring atomsselected from the group consisting of carbon, nitrogen, and oxygen; R⁶is selected from the group consisting of alkyl, haloalkyl, aryl,arylalkyl, heteroaryl, and heteroarylalkyl, each of which may beoptionally independently substituted with one or more substituentsselected from the group consisting of halogen, alkyl, alkoxy, haloalkyl,and haloalkoxy; or R⁵ and R⁶ together form a fused cycloalkyl orheterocycloalkyl ring having from 5 to 6 ring atoms selected from thegroup consisting of carbon, nitrogen, and oxygen; R⁷ and R⁸ areindependently selected from the group consisting of hydrogen, OH, andCH₃; and E is selected from the group consisting of S, O, N(H), N(CH₃),and CH₂.
 4. A method of controlling fungal pathogens, the methodcomprising administering to a plant, a seed or soil a compositioncomprising an effective amount of compound of Formula II or a saltthereof,

wherein R¹ is selected from the group consisting of a prodrug of acarboxylic acid and a carboxylic acid isostere; R² is selected from thegroup consisting of alkyl, cycloalkyl, heterocycloalkyl, aryl andheteroaryl, each of which may be optionally independently substitutedwith one or more substituents selected from the group consisting ofhalogen, CH₃, OCH₃, CF₃, OCF₃, and CN; R³ is selected from the groupconsisting of hydrogen, CN, ethynyl, CH₂N(R⁹R¹⁰), and C(O)N(R⁹R¹⁰),wherein R⁹ and R¹⁰ are each independently selected from the groupconsisting of hydrogen and alkyl; R⁴ is selected from the groupconsisting of haloalkyl, aryl, arylalkyl, heteroaryl, andheteroarylalkyl, each of which may be optionally independentlysubstituted with one or more substituents selected from the groupconsisting of halogen, alkyl, alkoxy, haloalkyl, haloalkoxy, alkenyl,hydroxyalky, hydroxy, N(R⁹R¹⁰), NR₁₁C(O)R¹², and O(CO)R¹³, wherein R⁹and R¹⁰ are independently selected from the group consisting of hydrogenand alkyl, R¹¹ is selected from the group consisting of hydrogen andalkyl, R¹² is alkyl, and R¹³ is alkyl; R⁵ is selected from the groupconsisting of hydrogen and alkyl; or R⁴ and R⁵ together form a fusedcycloalkyl or heterocycloalkyl ring having from 5 to 6 ring atomsselected from the group consisting of carbon, nitrogen, and oxygen; R⁶is selected from the group consisting of alkyl, haloalkyl, aryl,arylalkyl, heteroaryl, and heteroarylalkyl, each of which may beoptionally independently substituted with one or more substituentsselected from the group consisting of halogen, alkyl, alkoxy, haloalkyl,and haloalkoxy; or R⁵ and R⁶ together form a fused cycloalkyl orheterocycloalkyl ring having from 5 to 6 ring atoms selected from thegroup consisting of carbon, nitrogen, and oxygen; and E is selected fromthe group consisting of S, O, N(H), N(CH₃), and CH₂.
 5. The method ofclaim 4 wherein the compound is of Formula IIa or a salt thereof,

wherein R¹ is a carboxylic acid isostere; R² is selected from the groupconsisting of alkyl, cycloalkyl, heterocycloalkyl, aryl and heteroaryl,each of which may be optionally independently substituted with one ormore substituents selected from the group consisting of halogen, CH₃,OCH₃, CF₃, OCF₃, and CN; R³ is selected from the group consisting ofhydrogen, CN, ethynyl, CH₂N(R⁹R¹⁰), and C(O)N(R⁹R¹⁰), wherein R⁹ and R¹⁰are each independently selected from the group consisting of hydrogenand alkyl; R⁴ is selected from the group consisting of haloalkyl, aryl,arylalkyl, heteroaryl, and heteroarylalkyl, each of which may beoptionally independently substituted with one or more substituentsselected from the group consisting of halogen, alkyl, alkoxy, haloalkyl,haloalkoxy, alkenyl, hydroxyalky, hydroxy, N(R⁹R¹⁰), NR₁₁C(O)R¹², andO(CO)R¹³, wherein R⁹ and R¹⁰ are independently selected from the groupconsisting of hydrogen and alkyl, R¹¹ is selected from the groupconsisting of hydrogen and alkyl, R¹² is alkyl, and R¹³ is alkyl; R⁵ isselected from the group consisting of hydrogen and alkyl; or R⁴ and R⁵together form a fused cycloalkyl or heterocycloalkyl ring having from 5to 6 ring atoms selected from the group consisting of carbon, nitrogen,and oxygen; R⁶ is selected from the group consisting of alkyl,haloalkyl, aryl, arylalkyl, heteroaryl, and heteroarylalkyl, each ofwhich may be optionally independently substituted with one or moresubstituents selected from the group consisting of halogen, alkyl,alkoxy, haloalkyl, and haloalkoxy; or R⁵ and R⁶ together form a fusedcycloalkyl or heterocycloalkyl ring having from 5 to 6 ring atomsselected from the group consisting of carbon, nitrogen, and oxygen; andE is selected from the group consisting of S, O, N(H), N(CH₃), and CH₂.6. The method of claim 4 wherein the compound is of Formula IIb or asalt thereof,

wherein R¹ is a prodrug of carboxylic acid; R² is selected from thegroup consisting of alkyl, cycloalkyl, heterocycloalkyl, aryl andheteroaryl, each of which may be optionally independently substitutedwith one or more substituents selected from the group consisting ofhalogen, CH₃, OCH₃, CF₃, OCF₃, and CN; R³ is selected from the groupconsisting of hydrogen, CN, ethynyl, CH₂N(R⁹R¹⁰), and C(O)N(R⁹R¹⁰),wherein R⁹ and R¹⁰ are each independently selected from the groupconsisting of hydrogen and alkyl; R⁴ is selected from the groupconsisting of haloalkyl, aryl, arylalkyl, heteroaryl, andheteroarylalkyl, each of which may be optionally independentlysubstituted with one or more substituents selected from the groupconsisting of halogen, alkyl, alkoxy, haloalkyl, haloalkoxy, alkenyl,hydroxyalky, hydroxy, N(R⁹R¹⁰), NR₁₁C(O)R¹², and O(CO)R¹³, wherein R⁹and R¹⁰ are independently selected from the group consisting of hydrogenand alkyl, R¹¹ is selected from the group consisting of hydrogen andalkyl, R¹² is alkyl, and R¹³ is alkyl; R⁵ is selected from the groupconsisting of hydrogen or alkyl; or R⁴ and R⁵ together form a fusedcycloalkyl or heterocycloalkyl ring having from 5 to 6 ring atomsselected from the group consisting of carbon, nitrogen, and oxygen; R⁶is selected from the group consisting of alkyl, haloalkyl, aryl,arylalkyl, heteroaryl, and heteroarylalkyl, each of which may beoptionally independently substituted with one or more substituentsselected from the group consisting of halogen, alkyl, alkoxy, haloalkyl,and haloalkoxy; or R⁵ and R⁶ together form a fused cycloalkyl orheterocycloalkyl ring having from 5 to 6 ring atoms selected from thegroup consisting of carbon, nitrogen, and oxygen; and E is selected fromthe group consisting of S, O, N(H), N(CH₃), and CH₂.
 7. A method ofmodulating acetyl-CoA carboxylase (ACCase) in a biological organism, themethod comprising administering to the biological organism a compositioncomprising an effective amount of a compound of Formula I or a saltthereof,

wherein R¹ is selected from the group consisting of OH and N(R⁷R⁸),wherein R⁷ and R⁸ are independently selected from the group consistingof hydrogen, OH, and CH₃; R² is selected from the group consisting ofalkyl, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl, each of whichmay be optionally substituted with one or more substituents selectedfrom the group consisting of halogen, CH₃, OCH₃, CF₃, OCF₃, and CN; R³is selected from the group consisting of hydrogen, CN, ethynyl,CH₂N(R⁹R¹⁰), and C(O)N(R⁹R¹⁰), wherein R⁹ and R¹⁰ are each independentlyselected from the group consisting of hydrogen and alkyl; R⁴ is selectedfrom the group consisting of haloalkyl, aryl, arylalkyl, heteroaryl, andheteroarylalkyl, each of which may be optionally independentlysubstituted with one or more substituents selected from the groupconsisting of halogen, alkyl, alkoxy, haloalkyl, haloalkoxy, alkenyl,hydroxyalky, hydroxy, N(R⁹R¹⁰), NR¹¹C(O)R¹² and O(CO)R¹³, wherein R⁹ andR¹⁰ are independently selected from the group consisting of hydrogen andalkyl, R¹¹ is selected from the group consisting of hydrogen and alkyl,R¹² is alkyl, and R¹³ is alkyl; R⁵ is selected from the group consistingof hydrogen and alkyl; or R⁴ and R⁵ together form a fused cycloalkyl orheterocycloalkyl ring having from 5 to 6 ring atoms selected from thegroup consisting of carbon, nitrogen, and oxygen; R⁶ is selected fromthe group consisting of alkyl, haloalkyl, aryl, arylalkyl, heteroaryl,and heteroarylalkyl, each of which may be optionally independentlysubstituted with one or more substituents selected from the groupconsisting of halogen, alkyl, alkoxy, haloalkyl, and haloalkoxy; or R⁵and R⁶ together form a fused cycloalkyl or heterocycloalkyl ring havingfrom 5 to 6 ring atoms selected from the group consisting of carbon,nitrogen, and oxygen; and E is selected from the group consisting of S,O, N(H), N(CH₃), and CH₂.
 8. The method of claim 7 wherein the compoundis of Formula Ia or a salt thereof,

wherein R² is selected from the group consisting of alkyl, cycloalkyl,heterocycloalkyl, aryl and heteroaryl, each of which may be optionallyindependently substituted with one or more substituents selected fromthe group consisting of halogen, CH₃, OCH₃, CF₃, OCF₃, and CN; R³ isselected from the group consisting of hydrogen, CN, ethynyl,CH₂N(R⁹R¹⁰), and C(O)N(R⁹R¹⁰), wherein R⁹ and R¹⁰ are each independentlyselected from the group consisting of hydrogen and alkyl; R⁴ is selectedfrom the group consisting of haloalkyl, aryl, arylalkyl, heteroaryl, andheteroarylalkyl, each of which may be optionally independentlysubstituted with one or more substituents selected from the groupconsisting of halogen, alkyl, alkoxy, haloalkyl, haloalkoxy, alkenyl,hydroxyalkyl, hydroxyl, N(R⁹R¹⁰), NR¹¹C(O)R¹², and O(CO)R¹³, wherein R⁹and R¹⁰ are independently selected from the group consisting of hydrogenand alkyl, R¹¹ is selected from the group consisting of hydrogen andalkyl, R¹² is alkyl, and R¹³ is alkyl; R⁵ is selected from the groupconsisting of hydrogen and alkyl; or R⁴ and R⁵ together form a fusedcycloalkyl or heterocycloalkyl ring having from 5 to 6 ring atomsselected from the group consisting of carbon, nitrogen, and oxygen; R⁶is selected from the group consisting of alkyl, haloalkyl, aryl,arylalkyl, heteroaryl, and heteroarylalkyl, each of which may beoptionally independently substituted with one or more substituentsselected from the group consisting of halogen, alkyl, alkoxy, haloalkyl,and haloalkoxy; or R⁵ and R⁶ together form a fused cycloalkyl orheterocycloalkyl ring having from 5 to 6 ring atoms selected from thegroup consisting of carbon, nitrogen, and oxygen; and E is selected fromthe group consisting of S, O, N(H), N(CH₃), and CH₂.
 9. The method ofclaim 7 wherein the compound is of Formula Ib or a salt thereof,

wherein R² is selected from the group consisting of alkyl, cycloalkyl,heterocycloalkyl, aryl and heteroaryl, each of which may be optionallyindependently substituted with one or more substituents selected fromthe group consisting of halogen, CH₃, OCH₃, CF₃, OCF₃, and CN; R³ isselected from the group consisting of hydrogen, CN, ethynyl,CH₂N(R⁹R¹⁰), and C(O)N(R⁹R¹⁰), wherein R⁹ and R¹⁰ are each independentlyselected from the group consisting of hydrogen and alkyl; R⁴ is selectedfrom the group consisting of haloalkyl, aryl, arylalkyl, heteroaryl, andheteroarylalkyl, each of which may be optionally independentlysubstituted with one or more substituents selected from the groupconsisting of halogen, alkyl, alkoxy, haloalkyl, haloalkoxy, alkenyl,hydroxyalkyl, hydroxyl, N(R⁹R¹⁰), NR¹¹C(O)R¹², and O(CO)R¹³, wherein R⁹and R¹⁰ are independently selected from the group consisting of hydrogenand alkyl, R¹¹ is selected from the group consisting of hydrogen andalkyl, R¹² is alkyl, and R¹³ is alkyl; R⁵ is selected from the groupconsisting of hydrogen and alkyl; or R⁴ and R⁵ together form a fusedcycloalkyl or heterocycloalkyl ring having from 5 to 6 ring atomsselected from the group consisting of carbon, nitrogen, and oxygen; R⁶is selected from the group consisting of alkyl, haloalkyl, aryl,arylalkyl, heteroaryl, and heteroarylalkyl, each of which may beoptionally independently substituted with one or more substituentsselected from the group consisting of halogen, alkyl, alkoxy, haloalkyl,and haloalkoxy; or R⁵ and R⁶ together form a fused cycloalkyl orheterocycloalkyl ring having from 5 to 6 ring atoms selected from thegroup consisting of carbon, nitrogen, and oxygen; R⁷ and R⁸ areindependently selected from the group consisting of hydrogen, OH, andCH₃; and E is selected from the group consisting of S, O, N(H), N(CH₃),and CH₂.
 10. A method of modulating acetyl-CoA carboxylase (ACCase) in abiological organism, the method comprising administering to thebiological organism a composition comprising an effective amount of acompound of Formula II or a salt thereof,

wherein R¹ is selected from the group consisting of a prodrug of acarboxylic acid and a carboxylic acid isostere; R² is selected from thegroup consisting of alkyl, cycloalkyl, heterocycloalkyl, aryl andheteroaryl, each of which may be optionally independently substitutedwith one or more substituents selected from the group consisting ofhalogen, CH₃, OCH₃, CF₃, OCF₃, and CN; R³ is selected from the groupconsisting of hydrogen, CN, ethynyl, CH₂N(R⁹R¹⁰), and C(O)N(R⁹R¹⁰),wherein R⁹ and R¹⁰ are each independently selected from the groupconsisting of hydrogen and alkyl; R⁴ is selected from the groupconsisting of haloalkyl, aryl, arylalkyl, heteroaryl, andheteroarylalkyl, each of which may be optionally independentlysubstituted with one or more substituents selected from the groupconsisting of halogen, alkyl, alkoxy, haloalkyl, haloalkoxy, alkenyl,hydroxyalkyl, hydroxyl, N(R⁹R¹⁰), NR¹¹C(O)R¹², and O(CO)R¹³, wherein R⁹and R¹⁰ are independently selected from the group consisting of hydrogenand alkyl, R¹¹ is selected from the group consisting of hydrogen andalkyl, R¹² is alkyl, and R¹³ is alkyl; R⁵ is selected from the groupconsisting of hydrogen and alkyl; or R⁴ and R⁵ together form a fusedcycloalkyl or heterocycloalkyl ring having from 5 to 6 ring atomsselected from the group consisting of carbon, nitrogen, and oxygen; R⁶is selected from the group consisting of alkyl, haloalkyl, aryl,arylalkyl, heteroaryl, and heteroarylalkyl, each of which may beoptionally independently substituted with one or more substituentsselected from the group consisting of halogen, alkyl, alkoxy, haloalkyl,and haloalkoxy; or R⁵ and R⁶ together form a fused cycloalkyl orheterocycloalkyl ring having from 5 to 6 ring atoms selected from thegroup consisting of carbon, nitrogen, and oxygen; and E is selected fromthe group consisting of S, O, N(H), N(CH₃), and CH₂.
 11. The method ofclaim 10 wherein the compound is of Formula IIa or a salt thereof,

wherein R¹ is a carboxylic acid isostere; R² is selected from the groupconsisting of alkyl, cycloalkyl, heterocycloalkyl, aryl and heteroaryl,each of which may be optionally independently substituted with one ormore substituents selected from the group consisting of halogen, CH₃,OCH₃, CF₃, OCF₃, and CN; R³ is selected from the group consisting ofhydrogen, CN, ethynyl, CH₂N(R⁹R¹⁰), and C(O)N(R⁹R¹⁰), wherein R⁹ and R¹⁰are each independently selected from the group consisting of hydrogenand alkyl; R⁴ is selected from the group consisting of haloalkyl, aryl,arylalkyl, heteroaryl, and heteroarylalkyl, each of which may beoptionally independently substituted with one or more substituentsselected from the group consisting of halogen, alkyl, alkoxy, haloalkyl,haloalkoxy, alkenyl, hydroxyalky, hydroxy, N(R⁹R¹⁰), NR₁₁C(O)R¹², andO(CO)R¹³, wherein R⁹ and R¹⁰ are independently selected from the groupconsisting of hydrogen and alkyl, R¹¹ is selected from the groupconsisting of hydrogen and alkyl, R¹² is alkyl, and R¹³ is alkyl; R⁵ isselected from the group consisting of hydrogen and alkyl; or R⁴ and R⁵together form a fused cycloalkyl or heterocycloalkyl ring having from 5to 6 ring atoms selected from the group consisting of carbon, nitrogen,and oxygen; R⁶ is selected from the group consisting of alkyl,haloalkyl, aryl, arylalkyl, heteroaryl, and heteroarylalkyl, each ofwhich may be optionally independently substituted with one or moresubstituents selected from the group consisting of halogen, alkyl,alkoxy, haloalkyl, and haloalkoxy; or R⁵ and R⁶ together form a fusedcycloalkyl or heterocycloalkyl ring having from 5 to 6 ring atomsselected from the group consisting of carbon, nitrogen, and oxygen; andE is selected from the group consisting of S, O, N(H), N(CH₃), and CH₂.12. The method of claim 10 wherein the compound is of Formula IIb or asalt thereof,

wherein R¹ is a prodrug of carboxylic acid; R² is selected from thegroup consisting of alkyl, cycloalkyl, heterocycloalkyl, aryl andheteroaryl, each of which may be optionally independently substitutedwith one or more substituents selected from the group consisting ofhalogen, CH₃, OCH₃, CF₃, OCF₃, and CN; R³ is selected from the groupconsisting of hydrogen, CN, ethynyl, CH₂N(R⁹R¹⁰), and C(O)N(R⁹R¹⁰),wherein R⁹ and R¹⁰ are each independently selected from the groupconsisting of hydrogen and alkyl; R⁴ is selected from the groupconsisting of haloalkyl, aryl, arylalkyl, heteroaryl, andheteroarylalkyl, each of which may be optionally independentlysubstituted with one or more substituents selected from the groupconsisting of halogen, alkyl, alkoxy, haloalkyl, haloalkoxy, alkenyl,hydroxyalkyl, hydroxyl, N(R⁹R¹⁰), NR¹¹C(O)R¹², and O(CO)R¹³, wherein R⁹and R¹⁰ are independently selected from the group consisting of hydrogenand alkyl, R¹¹ is selected from the group consisting of hydrogen andalkyl, R¹² is alkyl, and R¹³ is alkyl; R⁵ is selected from the groupconsisting of hydrogen or alkyl; or R⁴ and R⁵ together form a fusedcycloalkyl or heterocycloalkyl ring having from 5 to 6 ring atomsselected from the group consisting of carbon, nitrogen, and oxygen; R⁶is selected from the group consisting of alkyl, haloalkyl, aryl,arylalkyl, heteroaryl, and heteroarylalkyl, each of which may beoptionally independently substituted with one or more substituentsselected from the group consisting of halogen, alkyl, alkoxy, haloalkyl,and haloalkoxy; or R⁵ and R⁶ together form a fused cycloalkyl orheterocycloalkyl ring having from 5 to 6 ring atoms selected from thegroup consisting of carbon, nitrogen, and oxygen; and E is selected fromthe group consisting of S, O, N(H), N(CH₃), and CH₂.
 13. The method ofclaim 1 or 7 wherein R¹ is OH.
 14. The method of any one of claims 1 to13 wherein R² is selected from the group consisting of aryl andheteroaryl, each of which may be optionally substituted with one or moresubstituents selected from the group consisting of halogen, CH₃, OCH₃,CF₃, OCF₃, and CN.
 15. The method of any one of claims 1 to 14 whereinR² is phenyl.
 16. The method of any one of claims 1 to 14 wherein R² isunsubstituted heteroaryl.
 17. The method of claim 16 wherein R² isselected from the group consisting of pyridyl, pyrimidyl, and thienyl.18. The method of any one of claims 1 to 17 wherein R³ is CN.
 19. Themethod of any one of claims 1 to 18 wherein R⁴ is selected from thegroup consisting of CF₃, thienyl, and optionally substituted phenyl. 20.The method of claim 19 wherein R⁴ is CF₃.
 21. The method of claim 19wherein R⁴ is thienyl.
 22. The method of claim 19 wherein R⁴ is phenyl.23. The method of claim 19 wherein R⁴ is selected from the groupconsisting of 4-halophenyl and 4-alkoxyphenyl.
 24. The method of any oneof claims 1 to 23 wherein R⁵ is hydrogen.
 25. The method of any one ofclaims 1 to 24 wherein R⁶ is selected from the group consisting ofmethyl, ethyl, thienyl, furanyl, and optionally substituted phenyl. 26.The method of claim 25 wherein R⁶ is thienyl.
 27. The method of claim 25wherein R⁶ is furanyl.
 28. The method of claim 25 wherein R⁶ is phenyl.29. The method of claim 25 wherein R⁶ is selected from the groupconsisting of 4-halophenyl and 4-alkoxyphenyl.
 30. The method of claim25 wherein R⁶ is disubstituted phenyl.
 31. The method of claim 25wherein R⁶ is selected from the group consisting of 2,4-dialkoxyphenylor 3,4-dialkoxyphenyl.
 32. The method of any one of claims 1 to 31wherein E is selected from the group consisting of S, O, and CH₂. 33.The method of claim 32 wherein E is S.
 34. The method of any one ofclaims 4, 5, 10, 11, or 13 to 33, wherein R¹ is a carboxylic acidisostere selected from the group consisting of tetrazolyl,aminosulfonyl, acylaminosulfonyl, methyl sulfonylcarbamyl,thiazolidinedionyl, oxazolidinedionyl, oxadiazolonyl, P(O)(OH)₂,P(O)(OH)H, and SO₃H.
 35. The method of any one of claims 4, 6, 10, or 12to 33 wherein R¹ is a prodrug of carboxylic acid selected from the groupconsisting of CH₂OH and ester group C(O)OR¹⁴ wherein R¹⁴ is selectedfrom the group consisting of methyl, ethyl, 2-oxopropyl,2-morpholinoethyl, and pivaloyloxymethyl.
 36. The method of claim 35wherein R¹ is C(O)OCH₃.
 37. The method of claim 35 wherein R¹ is CH₂OH.38. The method of claim 35 wherein R¹ is C(O)OCH₂CH₃.
 39. A method ofcontrolling fungal pathogens, the method comprising administering to aplant, a seed or soil a composition comprising an effective amount of acompound selected from the group consisting of:2-((4-(4-chlorophenyl)-3-cyano-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-(thiophen-2-yl)-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4,6-di(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetic acid,or a salt thereof,2-((3-cyano-4-phenyl-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-8-methyl-4-(thiophen-2-yl)-5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)thio)-2-phenylaceticacid,2-((4-cyano-1-(thiophen-2-yl)-5,6,7,8-tetrahydroisoquinolin-3-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-(2,4-dimethoxyphenyl)-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-(3,4-dimethoxyphenyl)-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((6-(4-bromophenyl)-3-cyano-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-(furan-2-yl)-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4,6-diphenylpyridin-2-yl)thio)-2-phenylacetic acid, or asalt thereof,2-((3-cyano-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((4-cyano-1-ethyl-5,6,7,8-tetrahydroisoquinolin-3-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-methyl-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-phenyl-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylaceticacid or a salt thereof,2-((4-(4-chlorophenyl)-3-cyano-5,6,7,8-tetrahydronaphthalen-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-(furan-2-yl)-4-(4-methoxyphenyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-(thiophen-2-yl)-4-(p-tolyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-(4-fluorophenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((4-(4-bromophenyl)-3-cyano-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-(furan-2-yl)-4-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4,6-di(furan-2-yl)pyridin-2-yl)thio)-2-phenylacetic acid, ora salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinolin-2-yl)oxy)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-6-(1-oxidothiophen-2-yl)pyridin-2-yl)oxy)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)butanoicacid, or a salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-6-(pyrimidin-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof2-((3-cyano-6-(3-methoxy-1-methyl-1H-pyrrol-2-yl)-4-(4-methoxyphenyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-(furan-2-yl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylacetamide,or a salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetamide,or a salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-N-hydroxy-2-phenylacetamide,or a salt thereof,4-(4-methoxyphenyl)-2-((phenyl(1H-tetrazol-5-yl)methyl)thio)-6-(thiophen-2-yl)nicotinonitrile,or a salt thereof,(((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)(phenyl)methyl)phosphonicacid, or a salt thereof,(((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)(phenyl)methyl)phosphinicacid, or a salt thereof,((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)(phenyl)methanesulfonicacid, or a salt thereof,((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)(phenyl)methanesulfonamide,or a salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-N-(methylsulfonyl)-2-phenylacetamide,or a salt thereof,2-(((2,4-dioxothiazolidin-5-yl)(phenyl)methyl)thio)-4-(4-methoxyphenyl)-6-(thiophen-2-yl)nicotinonitrile,or a salt thereof,2-(((2,4-dioxooxazolidin-5-yl)(phenyl)methyl)thio)-4-(4-methoxyphenyl)-6-(thiophen-2-yl)nicotinonitrile,or a salt thereof,4-(4-methoxyphenyl)-2-(((5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)(phenyl)methyl)thio)-6-(thiophen-2-yl)nicotinonitrile,or a salt thereof,2-((2-hydroxy-1-phenylethyl)thio)-4-(4-methoxyphenyl)-6-(thiophen-2-yl)nicotinonitrile,or a salt thereof,2-((2-hydroxy-1-phenylethyl)thio)-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinoline-3-carbonitrile,or a salt thereof, methyl2-((3-cyano-6-(thiophen-2-yl)-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylacetate,or a salt thereof, and4-(furan-2-yl)-2-(((2-hydroxy-1-phenylethyl)thio)-6-(thiophen-2-yl)nicotinonitrile,or a salt thereof.
 40. A method of modulating acetyl-CoA carboxylase(ACCase) in a biological organism, the method comprising administeringto the biological organism a composition comprising an effective amountof a compound selected from the group consisting of:2-((4-(4-chlorophenyl)-3-cyano-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-(thiophen-2-yl)-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4,6-di(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetic acid,or a salt thereof,2-((3-cyano-4-phenyl-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-8-methyl-4-(thiophen-2-yl)-5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)thio)-2-phenylaceticacid,2-((4-cyano-1-(thiophen-2-yl)-5,6,7,8-tetrahydroisoquinolin-3-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-(2,4-dimethoxyphenyl)-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-(3,4-dimethoxyphenyl)-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((6-(4-bromophenyl)-3-cyano-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-(furan-2-yl)-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4,6-diphenylpyridin-2-yl)thio)-2-phenylacetic acid, or asalt thereof,2-((3-cyano-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((4-cyano-1-ethyl-5,6,7,8-tetrahydroisoquinolin-3-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-methyl-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-phenyl-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylaceticacid or a salt thereof,2-((4-(4-chlorophenyl)-3-cyano-5,6,7,8-tetrahydronaphthalen-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-(furan-2-yl)-4-(4-methoxyphenyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-(thiophen-2-yl)-4-(p-tolyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-(4-fluorophenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((4-(4-bromophenyl)-3-cyano-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-6-(furan-2-yl)-4-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4,6-di(furan-2-yl)pyridin-2-yl)thio)-2-phenylacetic acid, ora salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinolin-2-yl)oxy)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-6-(1-oxidothiophen-2-yl)pyridin-2-yl)oxy)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)butanoicacid, or a salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-6-(pyrimidin-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof2-((3-cyano-6-(3-methoxy-1-methyl-1H-pyrrol-2-yl)-4-(4-methoxyphenyl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-(furan-2-yl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylaceticacid, or a salt thereof,2-((3-cyano-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinolin-2-yl)thio)-2-phenylacetamide,or a salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-2-phenylacetamide,or a salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-N-hydroxy-2-phenylacetamide,or a salt thereof,4-(4-methoxyphenyl)-2-((phenyl(1H-tetrazol-5-yl)methyl)thio)-6-(thiophen-2-yl)nicotinonitrile,or a salt thereof,(((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)(phenyl)methyl)phosphonicacid, or a salt thereof,(((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)(phenyl)methyl)phosphinicacid, or a salt thereof,((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)(phenyl)methanesulfonicacid, or a salt thereof,((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)(phenyl)methanesulfonamide,or a salt thereof,2-((3-cyano-4-(4-methoxyphenyl)-6-(thiophen-2-yl)pyridin-2-yl)thio)-N-(methylsulfonyl)-2-phenylacetamide,or a salt thereof,2-(((2,4-dioxothiazolidin-5-yl)(phenyl)methyl)thio)-4-(4-methoxyphenyl)-6-(thiophen-2-yl)nicotinonitrile,or a salt thereof,2-(((2,4-dioxooxazolidin-5-yl)(phenyl)methyl)thio)-4-(4-methoxyphenyl)-6-(thiophen-2-yl)nicotinonitrile,or a salt thereof,4-(4-methoxyphenyl)-2-(((5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)(phenyl)methyl)thio)-6-(thiophen-2-yl)nicotinonitrile,or a salt thereof,2-((2-hydroxy-1-phenylethyl)thio)-4-(4-methoxyphenyl)-6-(thiophen-2-yl)nicotinonitrile,or a salt thereof,2-((2-hydroxy-1-phenylethyl)thio)-4-(thiophen-2-yl)-5,6,7,8-tetrahydroquinoline-3-carbonitrile,or a salt thereof, methyl2-((3-cyano-6-(thiophen-2-yl)-4-(trifluoromethyl)pyridin-2-yl)thio)-2-phenylacetate,or a salt thereof, and4-(furan-2-yl)-2-((2-hydroxy-1-phenylethyl)thio)-6-(thiophen-2-yl)nicotinonitrile,or a salt thereof.
 41. The method of any one of claims 1 to 40, whereinthe method comprises administering the composition to a seed.
 42. Atreated seed prepared according to the method of claim
 41. 43. Themethod of any one of claims 1 to 40, wherein the method comprisesexogenously administering the composition to a plant.
 44. The method ofclaim 43 wherein the composition is applied to the foliage of a plant.45. The method of claim 43 wherein the method comprises applying thecomposition to the soil surrounding the root zone of a plant.
 46. Themethod of claim 43 wherein the composition is applied directly to thebase of the plants or to the soil immediately adjacent to the plants.47. The method of any one of claims 43 to 46 wherein the exogenoustreatment composition is applied such that it drains through the soil tothe root area of the plant.
 48. The method of any one of claims 43 to 47wherein the composition is applied using a drench application, dripirrigation technique, or tilled into the soil or applied in furrow
 49. Acompound of formula I, Ia, Ib, II, IIa, or IIb as set forth in any oneof claims 1 to
 48. 50. A treatment composition comprising an effectiveamount of a compound as set forth in claim
 49. 51. The treatmentcomposition of claim 50 further comprising a surfactant.
 52. Thetreatment composition of claim 50 further comprising a co-solvent. 53.The treatment composition of claim 50 further comprising a biologicalcontrol agent, microbial extract, natural product, plant growthactivator or plant defense agent or mixtures thereof.
 54. The treatmentcomposition of claim 53 wherein the biological control agent is selectedfrom the group consisting of bacteria, fungi, beneficial nematodes, andviruses.
 55. The treatment composition of claim 54 wherein thebiological control agent is a bacterium of the genus Actinomycetes,Agrobacterium, Arthrobacter, Alcaligenes, Aureobacterium, Azobacter,Beijerinckia, Brevibacillus, Burkholderia, Chromobacterium, Clostridium,Clavibacter, Comamonas, Corynebacterium, Curtobacterium, Enterobacter,Flavobacterium, Gluconobacter, Hydrogenophage, Klebsiella,Methylobacterium, Paenibacillus, Pasteuria, Photorhabdus,Phyllobacterium, Pseudomonas, Rhizobium, Serratia, Sphingobacterium,Stenotrophomonas, Variovax, and Xenorhabdus.
 56. The treatmentcomposition of claim 53 wherein the biological control agent is a plantgrowth activator or plant defense agent selected from the groupconsisting of harpin, Reynoutria sachalinensis, jasmonate,lipochitooligosaccharides, and isoflavones.
 57. The treatmentcomposition of any one of claims 50 to 56 further comprising a secondpesticide, wherein the second pesticide is selected from the groupconsisting of fungicides, insecticides and herbicides or mixturesthereof.
 58. The treatment composition of claim 57 wherein the secondpesticide is a fungicide selected from the group consisting ofacibenzolar-S-methyl, azoxystrobin, benalaxyl, bixafen, boscalid,carbendazim, cyproconazole, dimethomorph, epoxiconazole, fluopyram,fluoxastrobin, flutianil, flutolanil, fluxapyroxad, fosetyl-A1,ipconazole, isopyrazam, kresoxim-methyl, mefenoxam, metalaxyl,metconazole, myclobutanil, orysastrobin, penflufen, penthiopyrad,picoxystrobin, propiconazole, prothioconazole, pyraclostrobin, sedaxane,silthiofam, tebuconazole, thifluzamide, thiophanate, tolclofos-methyl,trifloxystrobin, and triticonazole.
 59. The treatment composition ofclaim 57 wherein the second pesticide is an insecticide or nematicideselected from the group consisting of abamectin, aldicarb, aldoxycarb,bifenthrin, carbofuran, chlorantraniliprole, clothianidin, cyfluthrin,cyhalothrin, cypermethrin, deltamethrin, dinotefuran, emamectin,ethiprole, fenamiphos, fipronil, flubendiamide, fosthiazate,imidacloprid, ivermectin, lambda-cyhalothrin, milbemectin,3-phenyl-5-(2-thienyl)-1,2,4-oxadiazole, nitenpyram, oxamyl, permethrin,spinetoram, spinosad, spirodichlofen, spirotetramat, tefluthrin,thiacloprid, thiamethoxam, and thiodicarb and mixtures thereof.
 60. Thetreatment composition of claim 57 wherein the second pesticide is anherbicide selected from the group consisting of acetochlor, clethodim,dicamba, flumioxazin, fomesafen, glyphosate, glufosinate, mesotrione,quizalofop, saflufenacil, sulcotrione, and 2,4-D and mixtures thereof.61. The treatment composition of claim 57 or 60 wherein the secondpesticide is an ACCase inhibitor.
 62. The treatment composition of claim61 wherein the second pesticide is an ACCase inhibitor selected from thegroup consisting of chlorazifop, clodinafop, clofop, cyhalofop,diclofop, fenoxaprop, fenoxaprop-P, fenthiaprop, fluazifop, fluazifop-P,haloxyfop, haloxyfop-P, isoxapyrifop, kuicaoxi, metamifop,propaquizafop, quizalofop, quizalofop-P, trifop, alloxydim, butroxydim,clethodim, cloproxydim, cycloxydim, profoxydim, sethoxydim,tepraloxydim, tralkoxydim, and pinoxaden.
 63. The treatment compositionof claim 61 wherein the second pesticide is selected from the groupconsisting of cycloxydim and sethoxydim.
 64. The treatment compositionof claim 57 wherein the second pesticide is selected from the groupconsisting of fluxapyroxad, ipconazole, metalaxyl, penflufen,pyraclostrobin, trifloxystrobin, abamectin, Bacillus firmus,clothianidin, imidacloprid, thiamethoxam and mixtures thereof.
 65. Thetreatment composition of claim 57 wherein the treatment compositioncomprises 3-phenyl-5-(thiophen-2-yl)-1,2,4-oxadiazole.
 66. A seedcomprising a coating comprising a compound as set forth in claim 49, ora composition as set forth in any one of claims 50 to
 65. 67. The seedof claim 66, wherein the coating comprises the compound in an amount ofat least about 0.005 mg/seed.
 68. The seed of claim 66, wherein thecoating comprises the compound in an amount of from about 0.005 to about1 mg/seed, or from about 0.05 to about 0.5 mg/seed.